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nsv6289784

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 124 SVs from 33 studies. See in: genome view    
Submitted genomic75,575,622-75,575,622Question Mark
Overlapping variant regions from other studies: 124 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):75,969,402-75,969,402Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6289784Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1275,575,62275,575,622
nsv6289784RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1275,969,40275,969,402

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17929847insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17929847Submitted genomicNC_000012.12:g.755
75622_75575623ins5
8
GRCh38 (hg38)NC_000012.12Chr1275,575,62275,575,622
nssv17929847RemappedPerfectNC_000012.11:g.759
69402_75969403ins5
8
GRCh37.p13First PassNC_000012.11Chr1275,969,40275,969,402

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)
nssv179298470.029571934
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