A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5969n100



Internal ID19016337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:57434214..60710125hg38UCSC Ensembl
chr6:57299012..57677872hg19UCSC Ensembl
chr6:57406971..57785831hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg383275912
hg19378861
hg18378861
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020177, nsv1031522, nsv1032663, nsv1025887
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)dgv5969n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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