A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982882



Internal ID12629021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143916494..144169439hg38UCSC Ensembl
Innerchr7:143613587..143866532hg19UCSC Ensembl
Innerchr7:143244520..143497465hg18UCSC Ensembl
Innerchr7:143051235..143304180hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38252946
hg19252946
hg18252946
hg17252946
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752147
Supporting Variants
SamplesBEC_607
Known GenesOR2A12, OR2A14, OR2A2, OR2A25, OR2A5, OR2F1, OR2F2, OR6B1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982882
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer