A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562438



Internal ID16349847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:80302458..80309511hg38UCSC Ensembl
Innerchr13:80876593..80883646hg19UCSC Ensembl
Innerchr13:79774594..79781647hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg387054
hg197054
hg187054
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv815985
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562438
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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