A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890902



Internal ID19185298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:89473670..89492658hg38UCSC Ensembl
Outerchr6:89473670..89492658hg38UCSC Ensembl
Innerchr6:90183389..90202377hg19UCSC Ensembl
Outerchr6:90183389..90202377hg19UCSC Ensembl
Innerchr6:90240108..90259096hg18UCSC Ensembl
Outerchr6:90240108..90259096hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3818989
hg1918989
hg1818989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780153
Samples
Known GenesANKRD6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890902
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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