A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982176



Internal ID12626618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2170636..2836436hg38UCSC Ensembl
Innerchr3:2212320..2878120hg19UCSC Ensembl
Innerchr3:2187320..2853120hg18UCSC Ensembl
Innerchr3:2187320..2853120hg17UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38665801
hg19665801
hg18665801
hg17665801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751993
Supporting Variants
SamplesBEC_40
Known GenesCNTN4
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982176
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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