A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782840



Internal ID19177857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:163972809..164029729hg38UCSC Ensembl
Innerchr2:164829319..164886239hg19UCSC Ensembl
Innerchr2:164537565..164594485hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3856921
hg1956921
hg1856921
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893505
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782840
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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