A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890879



Internal ID19185181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:74728511..74747387hg38UCSC Ensembl
Outerchr6:74728511..74747387hg38UCSC Ensembl
Innerchr6:75438227..75457103hg19UCSC Ensembl
Outerchr6:75438227..75457103hg19UCSC Ensembl
Innerchr6:75494947..75513823hg18UCSC Ensembl
Outerchr6:75494947..75513823hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3818877
hg1918877
hg1818877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780909
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890879
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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