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nsv590329

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,487

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 404 SVs from 77 studies. See in: genome view    
Remapped(Score: Perfect):52,995,193-53,003,679Question Mark
Overlapping variant regions from other studies: 403 SVs from 77 studies. See in: genome view    
Remapped(Score: Perfect):53,029,209-53,037,695Question Mark
Overlapping variant regions from other studies: 181 SVs from 24 studies. See in: genome view    
Submitted genomic53,004,249-53,012,735Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv590329RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr352,995,19353,003,679
nsv590329RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr353,029,20953,037,695
nsv590329Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000003.10Chr353,004,24953,012,735

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv963274copy number lossSNP arraySNP genotyping analysis

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv963274RemappedPerfectNC_000003.12:g.(?_
52995193)_(5300367
9_?)del
GRCh38.p12First PassNC_000003.12Chr352,995,19353,003,679
nssv963274RemappedPerfectNC_000003.11:g.(?_
53029209)_(5303769
5_?)del
GRCh37.p13First PassNC_000003.11Chr353,029,20953,037,695
nssv963274Submitted genomicNC_000003.10:g.(?_
53004249)_(5301273
5_?)del
NCBI36 (hg18)NC_000003.10Chr353,004,24953,012,735

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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