A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669789



Internal ID15059755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:78013628..78038182hg38UCSC Ensembl
Innerchr11:77724674..77749228hg19UCSC Ensembl
Innerchr11:77402322..77426876hg18UCSC Ensembl
Innerchr11:77402322..77426876hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3824555
hg1924555
hg1824555
hg1724555
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)nssv669789
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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