A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv772152



Internal ID16066108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:43984709..43993819hg38UCSC Ensembl
Innerchr11:44006259..44015369hg19UCSC Ensembl
Innerchr11:43962835..43971945hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg389111
hg199111
hg189111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554173
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)nssv772152
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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