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nsv5402440

  • 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: 94 SVs from 19 studies. See in: genome view    
Submitted genomic99,908,400-99,908,451Question Mark
Overlapping variant regions from other studies: 94 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):102,670,682-102,670,733Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5402440Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr999,908,40099,908,451
nsv5402440RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9102,670,682102,670,733

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17025534alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17025534Submitted genomicNC_000009.12:g.999
08400_99908451ins2
80
GRCh38 (hg38)NC_000009.12Chr999,908,40099,908,451
nssv17025534RemappedPerfectNC_000009.11:g.102
670682_102670733in
s280
GRCh37.p13First PassNC_000009.11Chr9102,670,682102,670,733

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)
nssv17025534<0.00116404
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