A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981666



Internal ID12972480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163020549..164074096hg38UCSC Ensembl
Innerchr3:162738337..163791884hg19UCSC Ensembl
Innerchr3:164221031..165274578hg18UCSC Ensembl
Innerchr3:164221039..165274586hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg381053548
hg191053548
hg181053548
hg171053548
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 Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981666
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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