A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562278



Internal ID16349687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:71657714..71713482hg38UCSC Ensembl
Innerchr13:72231846..72287614hg19UCSC Ensembl
Innerchr13:71129847..71185615hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3855769
hg1955769
hg1855769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv813835
Samples
Known GenesDACH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562278
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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