A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv813748



Internal ID16107704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70161932..70194552hg38UCSC Ensembl
Innerchr13:70736064..70768684hg19UCSC Ensembl
Innerchr13:69634065..69666685hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3832621
hg1932621
hg1832621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562232
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)nssv813748
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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