A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796768



Internal ID19182752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:124011148..124076857hg38UCSC Ensembl
Innerchr6:124332293..124398002hg19UCSC Ensembl
Innerchr6:124373992..124439701hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3865710
hg1965710
hg1865710
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890940
Supporting Variants
Samples
Known GenesNKAIN2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=19
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796768
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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