A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027528



Internal ID86057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97076668..97083616hg38UCSC Ensembl
chr9:99838950..99845898hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg386949
hg196949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492630
Supporting Variants
Samples
Known GenesLOC340508
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027528
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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