A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781071



Internal ID18828868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26369321..26433101hg38UCSC Ensembl
Innerchr6:26369549..26433329hg19UCSC Ensembl
Innerchr6:26477528..26541308hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3863781
hg1963781
hg1863781
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
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=21
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781071
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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