A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562952



Internal ID16003675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:99934267..99976973hg38UCSC Ensembl
Innerchr13:100586521..100629227hg19UCSC Ensembl
Innerchr13:99384522..99427228hg18UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3842707
hg1942707
hg1842707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv818127
Samples
Known GenesZIC5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562952
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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