A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16920892



Internal ID14705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:150472955..150473013hg38UCSC Ensembl
chr2:151329469..151329527hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437309
Supporting Variants
Samples
Known GenesRND3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16920892
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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