A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781723



Internal ID18813890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2603842..2664887hg38UCSC Ensembl
Innerchr3:2645526..2706571hg19UCSC Ensembl
Innerchr3:2620526..2681571hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3861046
hg1961046
hg1861046
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893622
Supporting Variants
Samples
Known GenesCNTN4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=38
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781723
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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