A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv782006



Internal ID15729276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:101919940..101987027hg38UCSC Ensembl
Innerchr11:101790671..101857758hg19UCSC Ensembl
Innerchr11:101295881..101362968hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3867088
hg1967088
hg1867088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556140
Supporting Variants
Samples
Known GenesKIAA1377
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv782006
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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