A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562501



Internal ID16349910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:82790687..82983723hg38UCSC Ensembl
Innerchr13:83364822..83557858hg19UCSC Ensembl
Innerchr13:82262823..82455859hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38193037
hg19193037
hg18193037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv816282
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562501
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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