A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv977358



Internal ID16271314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162149291..162231496hg38UCSC Ensembl
Innerchr3:161867079..161949284hg19UCSC Ensembl
Innerchr3:163349773..163431978hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3882206
hg1982206
hg1882206
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592149
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv977358
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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