A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705109



Internal ID15095075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:160053263..160106434hg38UCSC Ensembl
Innerchr1:160023053..160076224hg19UCSC Ensembl
Innerchr1:158289677..158342848hg18UCSC Ensembl
Innerchr1:156836126..156889297hg17UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg3853172
hg1953172
hg1853172
hg1753172
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520189
Supporting Variants
Samples
Known GenesIGSF8, KCNJ10, KCNJ9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705109
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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