A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778909



Internal ID19174075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105532207..105708865hg38UCSC Ensembl
Innerchr14:105998544..106175202hg19UCSC Ensembl
Innerchr14:105069589..105246247hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38176659
hg19176659
hg18176659
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892587
Supporting Variants
Samples
Known GenesELK2AP, MIR8071-1, MIR8071-2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=23
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778909
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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