A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562535



Internal ID16349944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83528305..83591536hg38UCSC Ensembl
Innerchr13:84102440..84165671hg19UCSC Ensembl
Innerchr13:83000441..83063672hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3863232
hg1963232
hg1863232
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3287n54
Supporting Variantsnssv816579, nssv816578, nssv816577, nssv1148547
SamplesHGDP01046
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562535
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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