A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5927n100



Internal ID20157543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26428086..26464561hg38UCSC Ensembl
chr6:26428314..26464789hg19UCSC Ensembl
chr6:26536293..26572768hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3836476
hg1936476
hg1836476
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030289, nsv1022309, nsv1029357
Samples
Known GenesBTN2A1, BTN2A3P, BTN3A3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5927n100
Frequency
Sample Size29084
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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