A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797618



Internal ID18817988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26369321..26442557hg38UCSC Ensembl
Innerchr6:26369549..26442785hg19UCSC Ensembl
Innerchr6:26477528..26550764hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3873237
hg1973237
hg1873237
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890802
Supporting Variants
Samples
Known GenesBTN2A2, BTN2A3P, BTN3A1, BTN3A2, BTN3A3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=62
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797618
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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