A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16908342



Internal ID6355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93333478..93333584hg38UCSC Ensembl
chr1:93799035..93799141hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425043
Supporting Variants
Samples
Known GenesLOC100131564
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16908342
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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