A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv809834



Internal ID16103790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:39360432..39361013hg38UCSC Ensembl
Innerchr13:39934569..39935150hg19UCSC Ensembl
Innerchr13:38832569..38833150hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38582
hg19582
hg18582
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561535
Supporting Variants
Samples
Known GenesLHFP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv809834
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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