A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662961



Internal ID15399613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67734155..67906211hg38UCSC Ensembl
Innerchr11:67501626..67673682hg19UCSC Ensembl
Innerchr11:67258202..67430258hg18UCSC Ensembl
Innerchr11:67258202..67430258hg17UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38172057
hg19172057
hg18172057
hg17172057
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516191
Supporting Variants
Samples
Known GenesFAM86C2P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662961
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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