A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985977



Internal ID12984328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19734966..19957752hg38UCSC Ensembl
Innerchr14:20203125..20425911hg19UCSC Ensembl
Innerchr14:19272965..19495751hg18UCSC Ensembl
Innerchr14:19272965..19495751hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38222787
hg19222787
hg18222787
hg17222787
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751218
Supporting Variants
SamplesSPC_93
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)essv6985977
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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