A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893624



Internal ID18837758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2417636..2779932hg38UCSC Ensembl
Outerchr3:2417636..2779932hg38UCSC Ensembl
Innerchr3:2459320..2821616hg19UCSC Ensembl
Outerchr3:2459320..2821616hg19UCSC Ensembl
Innerchr3:2434320..2796616hg18UCSC Ensembl
Outerchr3:2434320..2796616hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38362297
hg19362297
hg18362297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778818
Samples
Known GenesCNTN4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893624
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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