A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5967n100



Internal ID19016335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:57361384..60663649hg38UCSC Ensembl
chr6:57226182..57631396hg19UCSC Ensembl
chr6:57334141..57739355hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg383302266
hg19405215
hg18405215
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1023626, nsv1031558, nsv1030993, nsv1027292
Samples
Known GenesPRIM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5967n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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