A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890944



Internal ID19185340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:128538174..128637261hg38UCSC Ensembl
Outerchr6:128538174..128637261hg38UCSC Ensembl
Innerchr6:128859319..128958406hg19UCSC Ensembl
Outerchr6:128859319..128958406hg19UCSC Ensembl
Innerchr6:128901012..129000099hg18UCSC Ensembl
Outerchr6:128901012..129000099hg18UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg3899088
hg1999088
hg1899088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800618
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890944
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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