A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148692



Internal ID15856065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:111029653..111092591hg38UCSC Ensembl
Innerchr13:111682000..111744938hg19UCSC Ensembl
Innerchr13:110480001..110542939hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3862939
hg1962939
hg1862939
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563170
Supporting Variants
Samples1798860569_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148692
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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