A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5928n100



Internal ID20157544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26428086..26471368hg38UCSC Ensembl
chr6:26428314..26471596hg19UCSC Ensembl
chr6:26536293..26579575hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3843283
hg1943283
hg1843283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024222, nsv1023581, nsv1031229, nsv1034561, nsv1033003, nsv1024483, nsv1031238
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)dgv5928n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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