A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177209



Internal ID20744249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:48992030..48992241hg38UCSC Ensembl
chr16:49025941..49026152hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514775
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177209
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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