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nsv5523202

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:81

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 121 SVs from 23 studies. See in: genome view    
Submitted genomic33,795,491-33,795,571Question Mark
Overlapping variant regions from other studies: 121 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):34,286,396-34,286,476Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5523202Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1933,795,49133,795,571
nsv5523202RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1934,286,39634,286,476

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17722903deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17722903Submitted genomicNC_000019.10:g.337
95491_33795571del
GRCh38 (hg38)NC_000019.10Chr1933,795,49133,795,571
nssv17722903RemappedPerfectNC_000019.9:g.3428
6396_34286476del
GRCh37.p13First PassNC_000019.9Chr1934,286,39634,286,476

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)
nssv17722903<0.00156402
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