A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890802



Internal ID18838418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26370778..26433101hg38UCSC Ensembl
Outerchr6:26369321..26442557hg38UCSC Ensembl
Innerchr6:26371006..26433329hg19UCSC Ensembl
Outerchr6:26369549..26442785hg19UCSC Ensembl
Innerchr6:26478985..26541308hg18UCSC Ensembl
Outerchr6:26477528..26550764hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3873237
hg1973237
hg1873237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779646, essv25783460, essv25797340, essv25784489, essv25796184, essv25781071, essv25782938, essv25797124, essv25783608, essv25783052, essv25797618, essv25785360, essv25785141, essv25787161
Samples
Known GenesBTN2A2, BTN2A3P, BTN3A1, BTN3A2, BTN3A3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890802
Frequency
Sample Size3017
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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