A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5968n100



Internal ID19016336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:57361384..60843127hg38UCSC Ensembl
chr6:57226182..57810874hg19UCSC Ensembl
chr6:57334141..57918833hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg383481744
hg19584693
hg18584693
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027827, nsv1022933, nsv1024902, nsv1020366
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)dgv5968n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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