A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799650



Internal ID19166183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:106455568..106574299hg38UCSC Ensembl
Innerchr5:105791269..105910000hg19UCSC Ensembl
Innerchr5:105819168..105937899hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38118732
hg19118732
hg18118732
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890702
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799650
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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