A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562993



Internal ID16350402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103477582..103607458hg38UCSC Ensembl
Innerchr13:104129932..104259808hg19UCSC Ensembl
Innerchr13:102927933..103057809hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38129877
hg19129877
hg18129877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv818844
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562993
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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