A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891336



Internal ID19185732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:9743407..9900720hg38UCSC Ensembl
Outerchr8:9743407..9900720hg38UCSC Ensembl
Innerchr8:9600917..9758230hg19UCSC Ensembl
Outerchr8:9600917..9758230hg19UCSC Ensembl
Innerchr8:9638327..9795640hg18UCSC Ensembl
Outerchr8:9638327..9795640hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38157314
hg19157314
hg18157314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779048
Samples
Known GenesLINC00599, TNKS
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891336
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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