A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562637



Internal ID16350046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:88853238..88899808hg38UCSC Ensembl
Innerchr13:89505492..89552062hg19UCSC Ensembl
Innerchr13:88303493..88350063hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3846571
hg1946571
hg1846571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3302n54
Supporting Variantsnssv816815
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562637
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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