A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6180n100



Internal ID20157796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162238004..162421445hg38UCSC Ensembl
chr6:162659036..162842477hg19UCSC Ensembl
chr6:162579026..162762467hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38183442
hg19183442
hg18183442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021884, nsv1019900
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)dgv6180n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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