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nsv469834

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:141,886

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 463 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):13,874,062-14,015,947Question Mark
Overlapping variant regions from other studies: 464 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):15,985,942-16,127,827Question Mark
Overlapping variant regions from other studies: 1 SVs from 1 studies. See in: genome view    
Submitted genomic14,994,607-15,136,492Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv469834RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000024.10ChrY13,874,06214,015,947
nsv469834RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000024.9ChrY15,985,94216,127,827
nsv469834Submitted genomicNCBI34 (hg16)Primary AssemblyNC_000024.6ChrY14,994,60715,136,492

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1676309copy number gainBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv1676309RemappedPerfectNC_000024.10:g.(?_
13874062)_(1401594
7_?)dup
GRCh38.p12First PassNC_000024.10ChrY13,874,06214,015,947
nssv1676309RemappedPerfectNC_000024.9:g.(?_1
5985942)_(16127827
_?)dup
GRCh37.p13First PassNC_000024.9ChrY15,985,94216,127,827
nssv1676309Submitted genomicNC_000024.6:g.(?_1
4994607)_(15136492
_?)dup
NCBI34 (hg16)NC_000024.6ChrY14,994,60715,136,492

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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