A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901245



Internal ID1644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27962772..27962822hg38UCSC Ensembl
chr1:28289283..28289333hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5536973
Supporting Variants
Samples
Known GenesXKR8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901245
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001093


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