A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5942n100



Internal ID20157558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31385103..31513522hg38UCSC Ensembl
chr6:31352880..31481299hg19UCSC Ensembl
chr6:31460859..31589278hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38128420
hg19128420
hg18128420
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015252, nsv1033146, nsv1026211, nsv1018795, nsv1018716, nsv1028659, nsv1031241, nsv1032299, nsv1034727, nsv1023515, nsv1020595, nsv1030737
Samples
Known GenesHCG26, HCP5, MICA, MICB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5942n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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