A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026971



Internal ID85702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:103238637..103238704hg38UCSC Ensembl
chr9:106000919..106000986hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485051
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026971
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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