A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6176n100



Internal ID20157792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162161146..162762531hg38UCSC Ensembl
chr6:162582178..163183563hg19UCSC Ensembl
chr6:162502168..163103553hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38601386
hg19601386
hg18601386
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025396, nsv1029151
Samples
Known GenesPACRG, PARK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6176n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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