A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17706921



Internal ID130587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9355649..9355700hg38UCSC Ensembl
chr16:9449506..9449557hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg383301
hg193301
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555924
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17706921
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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