A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986296



Internal ID12629019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143875259..144169259hg38UCSC Ensembl
Innerchr7:143572352..143866352hg19UCSC Ensembl
Innerchr7:143203285..143497285hg18UCSC Ensembl
Innerchr7:143010000..143304000hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38294001
hg19294001
hg18294001
hg17294001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752147
Supporting Variants
SamplesBEC_607
Known GenesFAM115A, OR2A12, OR2A14, OR2A2, OR2A25, OR2A5, OR2F1, OR2F2, OR6B1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986296
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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