A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561895



Internal ID16349304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:62524863..62572937hg38UCSC Ensembl
Innerchr13:63098996..63147070hg19UCSC Ensembl
Innerchr13:61996997..62045071hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3848075
hg1948075
hg1848075
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv812456
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561895
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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