A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990748



Internal ID61244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:159773..160040hg38UCSC Ensembl
chr7:159773..160040hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467524
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990748
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.473406


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