A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556140



Internal ID15996863
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 StatusM
Merged Variants
Supporting Variantsnssv782006
Samples
Known GenesKIAA1377
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556140
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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