A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987434



Internal ID12629337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19735001..19987101hg38UCSC Ensembl
Innerchr14:20203160..20455260hg19UCSC Ensembl
Innerchr14:19273000..19525100hg18UCSC Ensembl
Innerchr14:19273000..19525100hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38252101
hg19252101
hg18252101
hg17252101
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751264
Supporting Variants
SamplesBEC_633
Known GenesOR4K1, OR4K15, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987434
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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