A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798396



Internal ID18816799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20876009..20931418hg38UCSC Ensembl
Innerchr14:21344168..21399577hg19UCSC Ensembl
Innerchr14:20414008..20469417hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3855410
hg1955410
hg1855410
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892467
Supporting Variants
Samples
Known GenesECRP, RNASE3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798396
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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