A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv772156



Internal ID16066112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:44089140..44093712hg38UCSC Ensembl
Innerchr11:44110690..44115262hg19UCSC Ensembl
Innerchr11:44067266..44071838hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg384573
hg194573
hg184573
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554177
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)nssv772156
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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