A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043773



Internal ID18786304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12697772..12716375hg38UCSC Ensembl
Innerchr16:12791629..12810232hg19UCSC Ensembl
Innerchr16:12699130..12717733hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3818604
hg1918604
hg1818604
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557221
Samples
Known GenesCPPED1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043773
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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