A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv818128



Internal ID16112084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:99967208..99986034hg38UCSC Ensembl
Innerchr13:100619462..100638288hg19UCSC Ensembl
Innerchr13:99417463..99436289hg18UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3818827
hg1918827
hg1818827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562954
Supporting Variants
Samples
Known GenesZIC2, ZIC5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv818128
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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