A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894113



Internal ID19184967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1895715..1934883hg38UCSC Ensembl
Outerchr5:1895715..1934883hg38UCSC Ensembl
Innerchr5:1895829..1934997hg19UCSC Ensembl
Outerchr5:1895829..1934997hg19UCSC Ensembl
Innerchr5:1948829..1987997hg18UCSC Ensembl
Outerchr5:1948829..1987997hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3839169
hg1939169
hg1839169
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790214
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894113
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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