A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16907456



Internal ID5758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:78686385..78686421hg38UCSC Ensembl
chr1:79152070..79152106hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535359
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16907456
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003903


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