A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152548



Internal ID15875478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145251103..145456796hg38UCSC Ensembl
Innerchr3:144968890..145174583hg19UCSC Ensembl
Innerchr3:146451580..146657273hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38205694
hg19205694
hg18205694
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591932
Supporting Variants
SamplesHGDP00688
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152548
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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