A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890940



Internal ID19185336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:124011148..124076857hg38UCSC Ensembl
Outerchr6:124011148..124076857hg38UCSC Ensembl
Innerchr6:124332293..124398002hg19UCSC Ensembl
Outerchr6:124332293..124398002hg19UCSC Ensembl
Innerchr6:124373992..124439701hg18UCSC Ensembl
Outerchr6:124373992..124439701hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3865710
hg1965710
hg1865710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796768
Samples
Known GenesNKAIN2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890940
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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