A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733894



Internal ID157560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9994000..10038071hg38UCSC Ensembl
chr21:10472028..10516099hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3844072
hg1944072
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428542
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733894
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.491231


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