A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703037



Internal ID15093003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:159920669..159932182hg38UCSC Ensembl
Innerchr1:159890459..159901972hg19UCSC Ensembl
Innerchr1:158157083..158168596hg18UCSC Ensembl
Innerchr1:156703532..156715045hg17UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg3811514
hg1911514
hg1811514
hg1711514
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516637
Supporting Variants
Samples
Known GenesIGSF9, TAGLN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703037
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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