A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670710



Internal ID15060676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:78020195..78052743hg38UCSC Ensembl
Innerchr11:77731241..77763789hg19UCSC Ensembl
Innerchr11:77408889..77441437hg18UCSC Ensembl
Innerchr11:77408889..77441437hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3832549
hg1932549
hg1832549
hg1732549
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516638
Supporting Variants
Samples
Known GenesKCTD14, NDUFC2-KCTD14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670710
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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