A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796972



Internal ID19166270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:62374928..62409118hg38UCSC Ensembl
Innerchr8:63287487..63321677hg19UCSC Ensembl
Innerchr8:63450041..63484231hg18UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3834191
hg1934191
hg1834191
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891405
Supporting Variants
Samples
Known GenesNKAIN3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796972
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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