A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16899121



Internal ID186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244113325..244113369hg38UCSC Ensembl
chr1:244276627..244276671hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5550028
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16899121
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.021404


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