A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17706792



Internal ID130458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2608000..2624100hg38UCSC Ensembl
chr16:2658001..2674101hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3816101
hg1916101
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5429203
Supporting Variants
Samples
Known GenesLOC652276
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17706792
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.478673


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