A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797816



Internal ID19177373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:102070965..102164718hg38UCSC Ensembl
Innerchr8:103083193..103176946hg19UCSC Ensembl
Innerchr8:103152369..103246122hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3893754
hg1993754
hg1893754
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891452
Supporting Variants
Samples
Known GenesMIR5680, NCALD
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=26
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797816
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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