A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781691



Internal ID19159566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:120847451..120940247hg38UCSC Ensembl
Innerchr5:120183146..120275942hg19UCSC Ensembl
Innerchr5:120211045..120303841hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3892797
hg1992797
hg1892797
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890727
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781691
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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