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nsv5544989

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:37

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 104 SVs from 24 studies. See in: genome view    
Submitted genomic137,898,332-137,898,368Question Mark
Overlapping variant regions from other studies: 104 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):137,583,078-137,583,114Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5544989Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7137,898,332137,898,368
nsv5544989RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7137,583,078137,583,114

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17003369insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17003369Submitted genomicNC_000007.14:g.137
898332_137898368in
s317
GRCh38 (hg38)NC_000007.14Chr7137,898,332137,898,368
nssv17003369RemappedPerfectNC_000007.13:g.137
583078_137583114in
s317
GRCh37.p13First PassNC_000007.13Chr7137,583,078137,583,114

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)
nssv17003369<0.00116404
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