A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060556



Internal ID18803087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:69954471..70152223hg38UCSC Ensembl
Innerchr16:69988374..70186126hg19UCSC Ensembl
Innerchr16:68545875..68743627hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38197753
hg19197753
hg18197753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2997n100
Supporting Variantsnssv3722731
Samples
Known GenesCLEC18A, 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)nsv1060556
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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