A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17020587



Internal ID81369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15250954..15252386hg38UCSC Ensembl
chr9:15250952..15252384hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg381433
hg191433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141440
Supporting Variants
Samples
Known GenesTTC39B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17020587
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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