A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561712



Internal ID16349121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55857016..55931047hg38UCSC Ensembl
Innerchr13:56431150..56505181hg19UCSC Ensembl
Innerchr13:55329151..55403182hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3874032
hg1974032
hg1874032
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176355
SamplesHGDP00214
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561712
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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