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nsv5554043

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:38

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 99 SVs from 24 studies. See in: genome view    
Submitted genomic37,657,730-37,657,767Question Mark
Overlapping variant regions from other studies: 99 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):38,053,737-38,053,774Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5554043Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2237,657,73037,657,767
nsv5554043RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2238,053,73738,053,774

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17728855sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17728855Submitted genomicNC_000022.11:g.376
57730_37657767ins5
57
GRCh38 (hg38)NC_000022.11Chr2237,657,73037,657,767
nssv17728855RemappedPerfectNC_000022.10:g.380
53737_38053774ins5
57
GRCh37.p13First PassNC_000022.10Chr2238,053,73738,053,774

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)
nssv17728855<0.00126404
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