A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988786



Internal ID12630108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19734966..19954424hg38UCSC Ensembl
Innerchr14:20203125..20422583hg19UCSC Ensembl
Innerchr14:19272965..19492423hg18UCSC Ensembl
Innerchr14:19272965..19492423hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38219459
hg19219459
hg18219459
hg17219459
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751268
Supporting Variants
SamplesBEC_688
Known GenesOR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988786
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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