A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562643



Internal ID16350052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:89731204..89834901hg38UCSC Ensembl
Innerchr13:90383458..90487155hg19UCSC Ensembl
Innerchr13:89181459..89285156hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38103698
hg19103698
hg18103698
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv816818
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562643
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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