A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890799



Internal ID19185101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:22741681..22747105hg38UCSC Ensembl
Outerchr6:22741681..22747105hg38UCSC Ensembl
Innerchr6:22741910..22747334hg19UCSC Ensembl
Outerchr6:22741910..22747334hg19UCSC Ensembl
Innerchr6:22849889..22855313hg18UCSC Ensembl
Outerchr6:22849889..22855313hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg385425
hg195425
hg185425
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780184
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890799
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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