A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782777



Internal ID18814860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20893225..20937726hg38UCSC Ensembl
Innerchr14:21361384..21405885hg19UCSC Ensembl
Innerchr14:20431224..20475725hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3844502
hg1944502
hg1844502
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892467
Supporting Variants
Samples
Known GenesECRP
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782777
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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