A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990452



Internal ID61042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:10000..38000hg38UCSC Ensembl
chr7:10001..38000hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3828001
hg1928000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142580
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990452
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001405


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