A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3006n100



Internal ID20154622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69990674..70219926hg38UCSC Ensembl
chr16:70024577..70253829hg19UCSC Ensembl
chr16:68582078..68811330hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38229253
hg19229253
hg18229253
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065057, nsv1056830, nsv1062900, nsv1061490
Samples
Known GenesCLEC18C, LOC100506060, MIR1972-1, MIR1972-2, PDPR, PDXDC2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3006n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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