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nsv884974

  • Variant Calls:3
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,653

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2174 SVs from 92 studies. See in: genome view    
Remapped(Score: Perfect):32,517,715-32,533,367Question Mark
Overlapping variant regions from other studies: 2174 SVs from 92 studies. See in: genome view    
Remapped(Score: Perfect):32,485,492-32,501,144Question Mark
Overlapping variant regions from other studies: 270 SVs from 21 studies. See in: genome view    
Remapped(Score: Good):3,821,149-3,836,625Question Mark
Overlapping variant regions from other studies: 1387 SVs from 33 studies. See in: genome view    
Submitted genomic32,593,470-32,609,122Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv884974RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr632,517,71532,521,32432,533,20732,533,367
nsv884974RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr632,485,49232,489,10132,500,98432,501,144
nsv884974RemappedGoodGRCh37.p13ALT_REF_LOCI_3Second PassNT_167245.1Chr6|NT_16
7245.1		-3,821,1493,836,625-
nsv884974Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000006.10Chr632,593,47032,597,07932,608,96232,609,122

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1526939copy number lossSP57986SNP arraySNP genotyping analysis9
nssv1554846copy number lossMS21036SNP arraySNP genotyping analysis15
nssv1590665copy number lossIS38549SNP arraySNP genotyping analysis15

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1526939RemappedPerfectNC_000006.12:g.(32
517715_32521324)_(
32533207_32533367)
del		GRCh38.p12First PassNC_000006.12Chr632,517,71532,521,32432,533,20732,533,367
nssv1554846RemappedPerfectNC_000006.12:g.(32
517715_32521324)_(
32533207_32533367)
del		GRCh38.p12First PassNC_000006.12Chr632,517,71532,521,32432,533,20732,533,367
nssv1590665RemappedPerfectNC_000006.12:g.(32
517715_32521324)_(
32533207_32533367)
del		GRCh38.p12First PassNC_000006.12Chr632,517,71532,521,32432,533,20732,533,367
nssv1526939RemappedGoodNT_167245.1:g.(?_3
821149)_(3836625_?
)delNT_167245.1:g.
(?_3821149)_(38366
25_?)del		GRCh37.p13Second PassNT_167245.1Chr6|NT_16
7245.1		-3,821,1493,836,625-
nssv1554846RemappedGoodNT_167245.1:g.(?_3
821149)_(3836625_?
)delNT_167245.1:g.
(?_3821149)_(38366
25_?)del		GRCh37.p13Second PassNT_167245.1Chr6|NT_16
7245.1		-3,821,1493,836,625-
nssv1590665RemappedGoodNT_167245.1:g.(?_3
821149)_(3836625_?
)delNT_167245.1:g.
(?_3821149)_(38366
25_?)del		GRCh37.p13Second PassNT_167245.1Chr6|NT_16
7245.1		-3,821,1493,836,625-
nssv1526939RemappedPerfectNC_000006.11:g.(32
485492_32489101)_(
32500984_32501144)
del		GRCh37.p13First PassNC_000006.11Chr632,485,49232,489,10132,500,98432,501,144
nssv1554846RemappedPerfectNC_000006.11:g.(32
485492_32489101)_(
32500984_32501144)
del		GRCh37.p13First PassNC_000006.11Chr632,485,49232,489,10132,500,98432,501,144
nssv1590665RemappedPerfectNC_000006.11:g.(32
485492_32489101)_(
32500984_32501144)
del		GRCh37.p13First PassNC_000006.11Chr632,485,49232,489,10132,500,98432,501,144
nssv1526939Submitted genomicNC_000006.10:g.(32
593470_32597079)_(
32608962_32609122)
del		NCBI36 (hg18)NC_000006.10Chr632,593,47032,597,07932,608,96232,609,122
nssv1554846Submitted genomicNC_000006.10:g.(32
593470_32597079)_(
32608962_32609122)
del		NCBI36 (hg18)NC_000006.10Chr632,593,47032,597,07932,608,96232,609,122
nssv1590665Submitted genomicNC_000006.10:g.(32
593470_32597079)_(
32608962_32609122)
del		NCBI36 (hg18)NC_000006.10Chr632,593,47032,597,07932,608,96232,609,122

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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