A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891400



Internal ID18839110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:56933474..57202184hg38UCSC Ensembl
Outerchr8:56933474..57202184hg38UCSC Ensembl
Innerchr8:57846033..58114743hg19UCSC Ensembl
Outerchr8:57846033..58114743hg19UCSC Ensembl
Innerchr8:58008587..58277297hg18UCSC Ensembl
Outerchr8:58008587..58277297hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38268711
hg19268711
hg18268711
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792004
Samples
Known GenesIMPAD1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891400
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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