A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16909193



Internal ID6913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16404836..16404898hg38UCSC Ensembl
chr2:16586104..16586166hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438932
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16909193
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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