A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv813690



Internal ID16107646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:69188811..69200965hg38UCSC Ensembl
Innerchr13:69762943..69775097hg19UCSC Ensembl
Innerchr13:68660944..68673098hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3812155
hg1912155
hg1812155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562205
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)nssv813690
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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