A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785281



Internal ID19171069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4080585..4188112hg38UCSC Ensembl
Innerchr3:4122269..4229796hg19UCSC Ensembl
Innerchr3:4097269..4204796hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38107528
hg19107528
hg18107528
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893628
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=29
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785281
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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