A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5867n100



Internal ID22791954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149649..254283hg38UCSC Ensembl
chr6:149649..254283hg19UCSC Ensembl
chr6:94649..199283hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38104635
hg19104635
hg18104635
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028995, nsv1027208, nsv1018408
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5867n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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