A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783382



Internal ID19171509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2999404..3025338hg38UCSC Ensembl
Innerchr5:2999518..3025452hg19UCSC Ensembl
Innerchr5:3052518..3078452hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3825935
hg1925935
hg1825935
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894115
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783382
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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