A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780965



Internal ID19170234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39380149..39532700hg38UCSC Ensembl
Innerchr8:39237668..39390219hg19UCSC Ensembl
Innerchr8:39356825..39509376hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38152552
hg19152552
hg18152552
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891382
Supporting Variants
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=20
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780965
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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