A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv771109



Internal ID16065065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38227656..38402577hg38UCSC Ensembl
Innerchr11:38249206..38424127hg19UCSC Ensembl
Innerchr11:38205782..38380703hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38174922
hg19174922
hg18174922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554040
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)nssv771109
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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