A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779048



Internal ID19179067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:9743407..9900720hg38UCSC Ensembl
Innerchr8:9600917..9758230hg19UCSC Ensembl
Innerchr8:9638327..9795640hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38157314
hg19157314
hg18157314
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891336
Supporting Variants
Samples
Known GenesLINC00599, TNKS
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=31
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779048
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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