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nsv5521504

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:863,075

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2790 SVs from 85 studies. See in: genome view    
Submitted genomic73,831,787-74,694,861Question Mark
Overlapping variant regions from other studies: 2790 SVs from 85 studies. See in: genome view    
Remapped(Score: Perfect):71,827,926-72,691,000Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5521504Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1773,831,78774,694,861
nsv5521504RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1771,827,92672,691,000

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714520duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714520Submitted genomicNC_000017.11:g.738
31787_74694861dup
GRCh38 (hg38)NC_000017.11Chr1773,831,78774,694,861
nssv17714520RemappedPerfectNC_000017.10:g.718
27926_72691000dup
GRCh37.p13First PassNC_000017.10Chr1771,827,92672,691,000

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17714520<0.00146404
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