A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6179n100



Internal ID20157795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162215411..162308495hg38UCSC Ensembl
chr6:162636443..162729527hg19UCSC Ensembl
chr6:162556433..162649517hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3893085
hg1993085
hg1893085
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022927, nsv1026704
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)dgv6179n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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