A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982881



Internal ID12629022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143879259..144167259hg38UCSC Ensembl
Innerchr7:143576352..143864352hg19UCSC Ensembl
Innerchr7:143207285..143495285hg18UCSC Ensembl
Innerchr7:143014000..143302000hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38288001
hg19288001
hg18288001
hg17288001
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 Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982881
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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