A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv820521



Internal ID15767791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113319297..113430196hg38UCSC Ensembl
Innerchr13:113973612..114084511hg19UCSC Ensembl
Innerchr13:113021613..113132512hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38110900
hg19110900
hg18110900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563318
Supporting Variants
Samples
Known GenesADPRHL1, GRTP1, LAMP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv820521
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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