A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16906547



Internal ID5154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101304496..101304496hg38UCSC Ensembl
chr1:101770052..101770052hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5543065
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16906547
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.090226


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