A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059489



Internal ID18802020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83126229..83147271hg38UCSC Ensembl
Innerchr16:83159834..83180876hg19UCSC Ensembl
Innerchr16:81717335..81738377hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3821043
hg1921043
hg1821043
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559863
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)nsv1059489
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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