A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981667



Internal ID12972491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163027420..164008569hg38UCSC Ensembl
Innerchr3:162745208..163726357hg19UCSC Ensembl
Innerchr3:164227902..165209051hg18UCSC Ensembl
Innerchr3:164227910..165209059hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38981150
hg19981150
hg18981150
hg17981150
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751982
Supporting Variants
SamplesBEC_314
Known GenesCT64
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981667
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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