A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056602



Internal ID18799133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:69954471..70085838hg38UCSC Ensembl
Innerchr16:69988374..70119741hg19UCSC Ensembl
Innerchr16:68545875..68677242hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38131368
hg19131368
hg18131368
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3722726
Samples
Known GenesCLEC18A, MIR1972-1, MIR1972-2, PDXDC2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056602
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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