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nsv5433145

  • 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: 137 SVs from 30 studies. See in: genome view    
Submitted genomic88,125,867-88,125,918Question Mark
Overlapping variant regions from other studies: 137 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):88,519,644-88,519,695Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5433145Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1288,125,86788,125,918
nsv5433145RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1288,519,64488,519,695

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17684005alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17684005Submitted genomicNC_000012.12:g.881
25867_88125918ins2
79
GRCh38 (hg38)NC_000012.12Chr1288,125,86788,125,918
nssv17684005RemappedPerfectNC_000012.11:g.885
19644_88519695ins2
79
GRCh37.p13First PassNC_000012.11Chr1288,519,64488,519,695

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)
nssv176840050.00186404
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