A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152226



Internal ID15876887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:54290..132831hg38UCSC Ensembl
Innerchr3:95973..174514hg19UCSC Ensembl
Innerchr3:70973..149514hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3878542
hg1978542
hg1878542
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589243
Supporting Variants
SamplesHGDP00909
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152226
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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