A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193874



Internal ID20760915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:521961..626139hg38UCSC Ensembl
chr16:571961..676139hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38104179
hg19104179
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506968
Supporting Variants
Samples
Known GenesC16orf11, CAPN15, LINC00235, MIR3176, MIR5587, NHLRC4, PIGQ, RAB11FIP3, RAB40C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193874
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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