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nsv5535058

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 144 SVs from 29 studies. See in: genome view    
Submitted genomic140,565,829-140,565,831Question Mark
Overlapping variant regions from other studies: 144 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):141,486,983-141,486,985Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5535058Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4140,565,829140,565,831
nsv5535058RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4141,486,983141,486,985

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16955370insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16955370Submitted genomicNC_000004.12:g.140
565829_140565831in
s72
GRCh38 (hg38)NC_000004.12Chr4140,565,829140,565,831
nssv16955370RemappedPerfectNC_000004.11:g.141
486983_141486985in
s72
GRCh37.p13First PassNC_000004.11Chr4141,486,983141,486,985

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)
nssv16955370<0.00136404
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