A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901202



Internal ID1613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27698405..27698405hg38UCSC Ensembl
chr1:28024916..28024916hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5398371
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901202
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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