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nsv5407979

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:26

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 87 SVs from 22 studies. See in: genome view    
Submitted genomic141,635,993-141,636,018Question Mark
Overlapping variant regions from other studies: 87 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):141,015,560-141,015,585Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5407979Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5141,635,993141,636,018
nsv5407979RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5141,015,560141,015,585

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16975434alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16975434Submitted genomicNC_000005.10:g.141
635993_141636018in
s281
GRCh38 (hg38)NC_000005.10Chr5141,635,993141,636,018
nssv16975434RemappedPerfectNC_000005.9:g.1410
15560_141015585ins
281
GRCh37.p13First PassNC_000005.9Chr5141,015,560141,015,585

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)
nssv16975434<0.00116404
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