A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5970n100



Internal ID22792057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:60444447..60731785hg38UCSC Ensembl
chr6:57412194..57699532hg19UCSC Ensembl
chr6:57520153..57807491hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg38287339
hg19287339
hg18287339
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022871, nsv1020737
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)dgv5970n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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