A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787360



Internal ID19167568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38893797..38904931hg38UCSC Ensembl
Innerchr22:39289802..39300936hg19UCSC Ensembl
Innerchr22:37619748..37630882hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3811135
hg1911135
hg1811135
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893483
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787360
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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