A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666549



Internal ID15403201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:66160302..66167718hg38UCSC Ensembl
Innerchr11:65927773..65935189hg19UCSC Ensembl
Innerchr11:65684349..65691765hg18UCSC Ensembl
Innerchr11:65684349..65691765hg17UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg387417
hg197417
hg187417
hg177417
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517090
Supporting Variants
Samples
Known GenesPACS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666549
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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