A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060011



Internal ID18802542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83118121..83160637hg38UCSC Ensembl
Innerchr16:83151726..83194242hg19UCSC Ensembl
Innerchr16:81709227..81751743hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3842517
hg1942517
hg1842517
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559862
Samples
Known GenesCDH13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060011
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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