A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779397



Internal ID18823966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89483618..89494527hg38UCSC Ensembl
Innerchr3:89532768..89543677hg19UCSC Ensembl
Innerchr3:89615458..89626367hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3810910
hg1910910
hg1810910
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893739
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779397
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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