A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176183



Internal ID15880626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:83085381..83125337hg38UCSC Ensembl
Innerchr11:82796423..82836379hg19UCSC Ensembl
Innerchr11:82474071..82514027hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3839957
hg1939957
hg1839957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555604
Supporting Variants
SamplesNINDS_236
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176183
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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