A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790020



Internal ID19170629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:13425011..14196025hg38UCSC Ensembl
Innerchr2:13565136..14336149hg19UCSC Ensembl
Innerchr2:13482587..14253600hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38771015
hg19771014
hg18771014
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891537
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=162
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790020
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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