A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561580



Internal ID16002303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:45810696..45881729hg38UCSC Ensembl
Innerchr13:46384831..46455864hg19UCSC Ensembl
Innerchr13:45282832..45353865hg18UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg3871034
hg1971034
hg1871034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv810011
Samples
Known GenesSIAH3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561580
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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