A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890945



Internal ID19185341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:130604622..130613626hg38UCSC Ensembl
Outerchr6:130604622..130613626hg38UCSC Ensembl
Innerchr6:130925767..130934771hg19UCSC Ensembl
Outerchr6:130925767..130934771hg19UCSC Ensembl
Innerchr6:130967460..130976464hg18UCSC Ensembl
Outerchr6:130967460..130976464hg18UCSC Ensembl
Cytoband6q23.1
Allele length
AssemblyAllele length
hg389005
hg199005
hg189005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781146
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890945
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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