A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5971n100



Internal ID22792058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:60568073..61119912hg38UCSC Ensembl
chr6:57535820..58145141hg19UCSC Ensembl
chr6:57643779..58253100hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg38551840
hg19609322
hg18609322
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030442, nsv1022139, nsv1016092, nsv1033968, nsv1024114, nsv1032764, nsv1016305, nsv1026093, nsv1020676, nsv1025740, nsv1028277, nsv1028100, nsv1031763, nsv1033363, nsv1024980
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)dgv5971n100
Frequency
Sample Size11257
Observed Gain30
Observed Loss0
Observed Complex0
Frequencyn/a


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