A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561539



Internal ID16002262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:41522908..41951740hg38UCSC Ensembl
Innerchr13:42097044..42525876hg19UCSC Ensembl
Innerchr13:40995044..41423876hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38428833
hg19428833
hg18428833
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175925
Samples1780862585_A
Known GenesMIR5006, VWA8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561539
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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