A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16910799



Internal ID7967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16817166..16817545hg38UCSC Ensembl
chr2:16998433..16998812hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555225
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16910799
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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