A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787161



Internal ID18830845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26370778..26436878hg38UCSC Ensembl
Innerchr6:26371006..26437106hg19UCSC Ensembl
Innerchr6:26478985..26545085hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3866101
hg1966101
hg1866101
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=23
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787161
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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