A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727187



Internal ID150853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45007760..45007792hg38UCSC Ensembl
chr21:46427675..46427707hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5550055
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727187
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.201998


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