A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981019



Internal ID12625990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2728826..2836436hg38UCSC Ensembl
Innerchr3:2770510..2878120hg19UCSC Ensembl
Innerchr3:2745510..2853120hg18UCSC Ensembl
Innerchr3:2745510..2853120hg17UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38107611
hg19107611
hg18107611
hg17107611
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751998
Supporting Variants
SamplesBEC_337
Known GenesCNTN4
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981019
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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