A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800639



Internal ID19163149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:62374928..62409119hg38UCSC Ensembl
Innerchr8:63287487..63321678hg19UCSC Ensembl
Innerchr8:63450041..63484232hg18UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3834192
hg1934192
hg1834192
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 HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800639
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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