A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506968



Internal ID20880256
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 StatusM
Merged Variants
Supporting Variantsnssv18193874
Samples
Known GenesC16orf11, CAPN15, LINC00235, MIR3176, MIR5587, NHLRC4, PIGQ, RAB11FIP3, RAB40C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506968
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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