A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16899417



Internal ID385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24302933..24303381hg38UCSC Ensembl
chr1:24629423..24629871hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38449
hg19449
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430363
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16899417
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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