A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv772151



Internal ID16066107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:43984709..43993454hg38UCSC Ensembl
Innerchr11:44006259..44015004hg19UCSC Ensembl
Innerchr11:43962835..43971580hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg388746
hg198746
hg188746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554172
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)nssv772151
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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