A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562782



Internal ID16350191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:96090029..96090541hg38UCSC Ensembl
Innerchr13:96742283..96742795hg19UCSC Ensembl
Innerchr13:95540284..95540796hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38513
hg19513
hg18513
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv817549, nssv817548, nssv817550
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562782
Frequency
Sample Size17421
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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