A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562646



Internal ID16350055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:90037521..90171605hg38UCSC Ensembl
Innerchr13:90689775..90823859hg19UCSC Ensembl
Innerchr13:89487776..89621860hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38134085
hg19134085
hg18134085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv816820
Samples
Known GenesLINC00559
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562646
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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