A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16910086



Internal ID7503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:14769145..14797735hg38UCSC Ensembl
chr2:14909269..14937859hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3828591
hg1928591
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559599
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16910086
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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