A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17020629



Internal ID81398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15597535..15626733hg38UCSC Ensembl
chr9:15597533..15626731hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3829199
hg1929199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5477870
Supporting Variants
Samples
Known GenesCCDC171
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17020629
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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