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nsv5534385

  • 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: 269 SVs from 32 studies. See in: genome view    
Submitted genomic124,483,688-124,483,739Question Mark
Overlapping variant regions from other studies: 269 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):125,495,929-125,495,980Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5534385Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8124,483,688124,483,739
nsv5534385RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8125,495,929125,495,980

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17017128insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17017128Submitted genomicNC_000008.11:g.124
483688_124483739in
s101
GRCh38 (hg38)NC_000008.11Chr8124,483,688124,483,739
nssv17017128RemappedPerfectNC_000008.10:g.125
495929_125495980in
s101
GRCh37.p13First PassNC_000008.10Chr8125,495,929125,495,980

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)
nssv17017128<0.00116404
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