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nsv5425646

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 117 SVs from 26 studies. See in: genome view    
Submitted genomic3,051,730-3,051,734Question Mark
Overlapping variant regions from other studies: 117 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):3,051,728-3,051,732Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5425646Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr193,051,7303,051,734
nsv5425646RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr193,051,7283,051,732

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17720516alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17720516Submitted genomicNC_000019.10:g.305
1730_3051734ins214
GRCh38 (hg38)NC_000019.10Chr193,051,7303,051,734
nssv17720516RemappedPerfectNC_000019.9:g.3051
728_3051732ins214
GRCh37.p13First PassNC_000019.9Chr193,051,7283,051,732

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)
nssv177205160.1388255976
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