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nsv590331

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,242

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 409 SVs from 77 studies. See in: genome view    
Remapped(Score: Perfect):52,996,726-53,004,967Question Mark
Overlapping variant regions from other studies: 408 SVs from 77 studies. See in: genome view    
Remapped(Score: Perfect):53,030,742-53,038,983Question Mark
Overlapping variant regions from other studies: 181 SVs from 24 studies. See in: genome view    
Submitted genomic53,005,782-53,014,023Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv590331RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr352,996,72653,004,967
nsv590331RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr353,030,74253,038,983
nsv590331Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000003.10Chr353,005,78253,014,023

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv963276copy number lossSNP arraySNP genotyping analysis

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv963276RemappedPerfectNC_000003.12:g.(?_
52996726)_(5300496
7_?)del
GRCh38.p12First PassNC_000003.12Chr352,996,72653,004,967
nssv963276RemappedPerfectNC_000003.11:g.(?_
53030742)_(5303898
3_?)del
GRCh37.p13First PassNC_000003.11Chr353,030,74253,038,983
nssv963276Submitted genomicNC_000003.10:g.(?_
53005782)_(5301402
3_?)del
NCBI36 (hg18)NC_000003.10Chr353,005,78253,014,023

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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