A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066763



Internal ID18809294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70015881..70179129hg38UCSC Ensembl
Innerchr16:70049784..70213032hg19UCSC Ensembl
Innerchr16:68607285..68770533hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38163249
hg19163249
hg18163249
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3005n100
Supporting Variantsnssv3559507, nssv3559509, nssv3559508, nssv3722742
Samples
Known GenesCLEC18C, 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)nsv1066763
Frequency
Sample Size29084
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer