A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786297



Internal ID19176639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105601281..105699778hg38UCSC Ensembl
Innerchr14:106067618..106166115hg19UCSC Ensembl
Innerchr14:105138663..105237160hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3898498
hg1998498
hg1898498
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=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786297
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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