A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175986



Internal ID15879831
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
SamplesNINDS_114
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175986
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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