A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5938n100



Internal ID20157554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29865090..29913570hg38UCSC Ensembl
chr6:29832867..29881347hg19UCSC Ensembl
chr6:29940846..29989326hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3848481
hg1948481
hg1848481
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1029680, nsv1021072
Samples
Known GenesHLA-H
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5938n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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