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nsv5525971

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:209

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 114 SVs from 15 studies. See in: genome view    
Submitted genomic32,434,189-32,434,397Question Mark
Overlapping variant regions from other studies: 114 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):32,925,095-32,925,303Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5525971Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1932,434,18932,434,397
nsv5525971RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1932,925,09532,925,303

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17722817deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17722817Submitted genomicNC_000019.10:g.324
34189_32434397del
GRCh38 (hg38)NC_000019.10Chr1932,434,18932,434,397
nssv17722817RemappedPerfectNC_000019.9:g.3292
5095_32925303del
GRCh37.p13First PassNC_000019.9Chr1932,925,09532,925,303

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)
nssv17722817<0.00126404
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