A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891405



Internal ID19185801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:62374928..62409118hg38UCSC Ensembl
Outerchr8:62374928..62409119hg38UCSC Ensembl
Innerchr8:63287487..63321677hg19UCSC Ensembl
Outerchr8:63287487..63321678hg19UCSC Ensembl
Innerchr8:63450041..63484231hg18UCSC Ensembl
Outerchr8:63450041..63484232hg18UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3834192
hg1934192
hg1834192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800639, essv25796972
Samples
Known GenesNKAIN3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891405
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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