A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv816602



Internal ID16110558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83607159..83741015hg38UCSC Ensembl
Innerchr13:84181294..84315150hg19UCSC Ensembl
Innerchr13:83079295..83213151hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38133857
hg19133857
hg18133857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562551
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)nssv816602
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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