A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891376



Internal ID19185772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:24680734..24777257hg38UCSC Ensembl
Outerchr8:24678673..24777257hg38UCSC Ensembl
Innerchr8:24538247..24634770hg19UCSC Ensembl
Outerchr8:24536186..24634770hg19UCSC Ensembl
Innerchr8:24594137..24690660hg18UCSC Ensembl
Outerchr8:24592076..24690660hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3898585
hg1998585
hg1898585
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779709, essv25796245, essv25799295
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891376
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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