A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148691



Internal ID15853271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:111025082..111096769hg38UCSC Ensembl
Innerchr13:111677429..111749116hg19UCSC Ensembl
Innerchr13:110475430..110547117hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3871688
hg1971688
hg1871688
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563167
Supporting Variants
Samples1780854058_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148691
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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