A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768955



Internal ID16062911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:23547614..23655700hg38UCSC Ensembl
Innerchr11:23569160..23677246hg19UCSC Ensembl
Innerchr11:23525736..23633822hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38108087
hg19108087
hg18108087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553760
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv768955
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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