A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066093



Internal ID18808624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70015881..70118407hg38UCSC Ensembl
Innerchr16:70049784..70152310hg19UCSC Ensembl
Innerchr16:68607285..68709811hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38102527
hg19102527
hg18102527
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3003n100
Supporting Variantsnssv3559499, nssv3722740
Samples
Known GenesMIR1972-1, 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)nsv1066093
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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