A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901932



Internal ID2087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31852877..31852916hg38UCSC Ensembl
chr1:32318478..32318517hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5542371
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901932
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001249


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