A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561537



Internal ID16002260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:40159719..40200730hg38UCSC Ensembl
Innerchr13:40733856..40774867hg19UCSC Ensembl
Innerchr13:39631856..39672867hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3841012
hg1941012
hg1841012
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv809836
Samples
Known GenesLINC00332, LINC00548
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561537
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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