A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891452



Internal ID19185848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:102070965..102164718hg38UCSC Ensembl
Outerchr8:102070965..102164718hg38UCSC Ensembl
Innerchr8:103083193..103176946hg19UCSC Ensembl
Outerchr8:103083193..103176946hg19UCSC Ensembl
Innerchr8:103152369..103246122hg18UCSC Ensembl
Outerchr8:103152369..103246122hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3893754
hg1993754
hg1893754
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797816
Samples
Known GenesMIR5680, NCALD
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891452
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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