A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv807428



Internal ID16101384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:32939884..32957890hg38UCSC Ensembl
Innerchr13:33514022..33532028hg19UCSC Ensembl
Innerchr13:32412022..32430028hg18UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3818007
hg1918007
hg1818007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561433
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)nssv807428
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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