A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890864



Internal ID19185166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:64318096..64346918hg38UCSC Ensembl
Outerchr6:64318096..64346918hg38UCSC Ensembl
Innerchr6:65027989..65056811hg19UCSC Ensembl
Outerchr6:65027989..65056811hg19UCSC Ensembl
Innerchr6:65085948..65114770hg18UCSC Ensembl
Outerchr6:65085948..65114770hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3828823
hg1928823
hg1828823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785861
Samples
Known GenesEYS
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890864
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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