A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780227



Internal ID19180168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:3004057..3025338hg38UCSC Ensembl
Innerchr5:3004171..3025452hg19UCSC Ensembl
Innerchr5:3057171..3078452hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3821282
hg1921282
hg1821282
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=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780227
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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