A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785368



Internal ID19179294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:95089558..95097142hg38UCSC Ensembl
Innerchr8:96101786..96109370hg19UCSC Ensembl
Innerchr8:96170962..96178546hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg387585
hg197585
hg187585
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891443
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785368
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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