A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655349



Internal ID15045315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:159920669..159938603hg38UCSC Ensembl
Innerchr1:159890459..159908393hg19UCSC Ensembl
Innerchr1:158157083..158175017hg18UCSC Ensembl
Innerchr1:156703532..156721466hg17UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg3817935
hg1917935
hg1817935
hg1717935
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)nssv655349
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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