A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6193n100



Internal ID20157809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162586362..162619009hg38UCSC Ensembl
chr6:163007394..163040041hg19UCSC Ensembl
chr6:162927384..162960031hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3832648
hg1932648
hg1832648
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015617, nsv1031834, nsv1034499
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)dgv6193n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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