A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv807647



Internal ID16101603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:34240750..34368738hg38UCSC Ensembl
Innerchr13:34814887..34942875hg19UCSC Ensembl
Innerchr13:33712887..33840875hg18UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg38127989
hg19127989
hg18127989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561461
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv807647
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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