A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191718



Internal ID20758758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:7751424..7820420hg38UCSC Ensembl
chr16:7801426..7870422hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3868997
hg1968997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515559
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191718
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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