A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16914668



Internal ID10527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:71840663..71841443hg38UCSC Ensembl
chr2:72067793..72068573hg19UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg38781
hg19781
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563163
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16914668
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001873


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