A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039336



Internal ID93946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119652195..119652258hg38UCSC Ensembl
chr10:121411707..121411770hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503299
Supporting Variants
Samples
Known GenesBAG3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039336
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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