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nsv5402785

  • 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: 102 SVs from 21 studies. See in: genome view    
Submitted genomic102,138,950-102,139,001Question Mark
Overlapping variant regions from other studies: 102 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):102,755,410-102,755,461Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5402785Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2102,138,950102,139,001
nsv5402785RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2102,755,410102,755,461

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16916406alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16916406Submitted genomicNC_000002.12:g.102
138950_102139001in
s243
GRCh38 (hg38)NC_000002.12Chr2102,138,950102,139,001
nssv16916406RemappedPerfectNC_000002.11:g.102
755410_102755461in
s243
GRCh37.p13First PassNC_000002.11Chr2102,755,410102,755,461

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)
nssv16916406<0.00146404
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