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nsv5428252

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 164 SVs from 31 studies. See in: genome view    
Submitted genomic75,675,573-75,675,624Question Mark
Overlapping variant regions from other studies: 164 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):75,967,914-75,967,965Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5428252Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1575,675,57375,675,624
nsv5428252RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1575,967,91475,967,965

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17702477alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17702477Submitted genomicNC_000015.10:g.756
75573_75675624ins2
78
GRCh38 (hg38)NC_000015.10Chr1575,675,57375,675,624
nssv17702477RemappedPerfectNC_000015.9:g.7596
7914_75967965ins27
8
GRCh37.p13First PassNC_000015.9Chr1575,967,91475,967,965

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)
nssv17702477<0.00126404
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