A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152018



Internal ID15854628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100635680..100714748hg38UCSC Ensembl
Innerchr3:100354524..100433592hg19UCSC Ensembl
Innerchr3:101837214..101916282hg18UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg3879069
hg1979069
hg1879069
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591166
Supporting Variants
Samples1780862246_A
Known GenesGPR128, TFG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152018
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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