A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6168n100



Internal ID22792255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161391387..161439604hg38UCSC Ensembl
chr6:161812419..161860636hg19UCSC Ensembl
chr6:161732409..161780626hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3848218
hg1948218
hg1848218
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018065, nsv1022345, nsv1024921, nsv1023319, nsv1018466, nsv1033192
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)dgv6168n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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