A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16935375



Internal ID24301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109381044..109388352hg38UCSC Ensembl
chr3:109099891..109107199hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg387309
hg197309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5441447
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16935375
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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