A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792604



Internal ID19182258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19745778..19955706hg38UCSC Ensembl
Innerchr14:20213937..20423865hg19UCSC Ensembl
Innerchr14:19283777..19493705hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38209929
hg19209929
hg18209929
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892451
Supporting Variants
Samples
Known GenesOR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=19
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792604
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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