A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780214



Internal ID19164576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8400590..8513610hg38UCSC Ensembl
Innerchr8:8258100..8371120hg19UCSC Ensembl
Innerchr8:8295510..8408530hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38113021
hg19113021
hg18113021
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891327
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=43
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780214
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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