A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6182n100



Internal ID20157798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162281800..162618151hg38UCSC Ensembl
chr6:162702832..163039183hg19UCSC Ensembl
chr6:162622822..162959173hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38336352
hg19336352
hg18336352
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026362, nsv1025211, nsv1017053, nsv1020080, nsv1027673
Samples
Known GenesPARK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6182n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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