A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17710517



Internal ID134183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88277268..88281757hg38UCSC Ensembl
chr16:88310874..88315363hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg384490
hg194490
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145116
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17710517
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.014944


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