A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893775



Internal ID19184595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:135829907..135890709hg38UCSC Ensembl
Outerchr3:135829907..135890709hg38UCSC Ensembl
Innerchr3:135548749..135609551hg19UCSC Ensembl
Outerchr3:135548749..135609551hg19UCSC Ensembl
Innerchr3:137031439..137092241hg18UCSC Ensembl
Outerchr3:137031439..137092241hg18UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3860803
hg1960803
hg1860803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796527
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893775
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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