A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6170n100



Internal ID20157786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161787295..161914435hg38UCSC Ensembl
chr6:162208327..162335467hg19UCSC Ensembl
chr6:162128317..162255457hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38127141
hg19127141
hg18127141
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031892, nsv1017037
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)dgv6170n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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