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nsv4652865

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:160,623

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 2922 SVs from 104 studies. See in: genome view    
Remapped(Score: Perfect):78,183,091-78,343,713Question Mark
Overlapping variant regions from other studies: 2922 SVs from 104 studies. See in: genome view    
Submitted genomic78,892,808-79,053,430Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4652865RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr678,183,09178,343,713
nsv4652865Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr678,892,80879,053,430

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16191504copy number lossCuratedCurated

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16191504RemappedPerfectNC_000006.12:g.781
83091_78343713del
GRCh38.p12First PassNC_000006.12Chr678,183,09178,343,713
nssv16191504Submitted genomicNC_000006.11:g.788
92808_79053430del
GRCh37 (hg19)NC_000006.11Chr678,892,80879,053,430

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv161915040.1457285008
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