A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931128



Internal ID21503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15307145..15308317hg38UCSC Ensembl
chr3:15348652..15349824hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg381173
hg191173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5434816
Supporting Variants
Samples
Known GenesSH3BP5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931128
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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