A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17011436



Internal ID75278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:50353161..50372411hg38UCSC Ensembl
chr8:51265721..51284971hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3819251
hg1919251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490193
Supporting Variants
Samples
Known GenesSNTG1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17011436
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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