A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985634



Internal ID12972495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163020510..163994510hg38UCSC Ensembl
Innerchr3:162738298..163712298hg19UCSC Ensembl
Innerchr3:164220992..165194992hg18UCSC Ensembl
Innerchr3:164221000..165195000hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38974001
hg19974001
hg18974001
hg17974001
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)essv6985634
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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