A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169839



Internal ID21313650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89448633..89494874hg38UCSC Ensembl
Outerchr16:89447775..89497312hg38UCSC Ensembl
Innerchr16:89515041..89561282hg19UCSC Ensembl
Outerchr16:89514183..89563720hg19UCSC Ensembl
Innerchr16:88042542..88088783hg18UCSC Ensembl
Outerchr16:88041684..88091221hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3849538
hg1949538
hg1849538
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14245915
SamplesPML_4
Known GenesANKRD11
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169839
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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