A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16917511



Internal ID12423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:90371992..90402400hg38UCSC Ensembl
chr2:90371637..90402045hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3830409
hg1930409
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432722
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16917511
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.5


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