A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16944284



Internal ID30191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196641206..196642219hg38UCSC Ensembl
chr3:196368077..196369090hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381014
hg191014
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5439942
Supporting Variants
Samples
Known GenesNRROS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16944284
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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