A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890767



Internal ID19185069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:171775013..171787475hg38UCSC Ensembl
Outerchr5:171775013..171787475hg38UCSC Ensembl
Innerchr5:171202017..171214479hg19UCSC Ensembl
Outerchr5:171202017..171214479hg19UCSC Ensembl
Innerchr5:171134622..171147084hg18UCSC Ensembl
Outerchr5:171134622..171147084hg18UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3812463
hg1912463
hg1812463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797144
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890767
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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