A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790214



Internal ID19174956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1895715..1934883hg38UCSC Ensembl
Innerchr5:1895829..1934997hg19UCSC Ensembl
Innerchr5:1948829..1987997hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3839169
hg1939169
hg1839169
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894113
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790214
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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