A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668719



Internal ID15058685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:78165443..78209884hg38UCSC Ensembl
Innerchr11:77876489..77920930hg19UCSC Ensembl
Innerchr11:77554137..77598578hg18UCSC Ensembl
Innerchr11:77554137..77598578hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3844442
hg1944442
hg1844442
hg1744442
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516503
Supporting Variants
Samples
Known GenesKCTD21, KCTD21-AS1, USP35
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668719
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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