A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891423



Internal ID19185819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:82124176..82946696hg38UCSC Ensembl
Outerchr8:82121871..83244363hg38UCSC Ensembl
Innerchr8:83036411..83858931hg19UCSC Ensembl
Outerchr8:83034106..84156598hg19UCSC Ensembl
Innerchr8:83198966..84021486hg18UCSC Ensembl
Outerchr8:83196661..84319153hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg381122493
hg191122493
hg181122493
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792196, essv25787963
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891423
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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