A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3722731



Internal ID18674326
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 StatusS
Merged Variantsnsv1060556
Supporting Variants
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)nssv3722731
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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