A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983283



Internal ID12628442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19735001..20095701hg38UCSC Ensembl
Innerchr14:20203160..20563860hg19UCSC Ensembl
Innerchr14:19273000..19633700hg18UCSC Ensembl
Innerchr14:19273000..19633700hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38360701
hg19360701
hg18360701
hg17360701
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751265
Supporting Variants
SamplesBEC_563
Known GenesOR4K1, OR4K13, OR4K14, OR4K15, OR4K2, OR4K5, OR4L1, OR4M1, OR4N2, OR4Q3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983283
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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