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nsv5475490

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:160

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1230 SVs from 79 studies. See in: genome view    
Submitted genomic39,502,621-39,502,780Question Mark
Overlapping variant regions from other studies: 1230 SVs from 79 studies. See in: genome view    
Remapped(Score: Perfect):39,360,140-39,360,299Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5475490Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr839,502,62139,502,780
nsv5475490RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr839,360,14039,360,299

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17010715duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17010715Submitted genomicNC_000008.11:g.395
02621_39502780dup
GRCh38 (hg38)NC_000008.11Chr839,502,62139,502,780
nssv17010715RemappedPerfectNC_000008.10:g.393
60140_39360299dup
GRCh37.p13First PassNC_000008.10Chr839,360,14039,360,299

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)
nssv17010715<0.00126404
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