A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901761



Internal ID1968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:43065910..43065944hg38UCSC Ensembl
chr1:43531581..43531615hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5407957
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901761
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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