A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784905



Internal ID18833054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103788746..103866422hg38UCSC Ensembl
Innerchr14:104255083..104332759hg19UCSC Ensembl
Innerchr14:103324836..103402512hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3877677
hg1977677
hg1877677
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892582
Supporting Variants
Samples
Known GenesLINC00637, PPP1R13B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784905
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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