A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17020611



Internal ID81388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15477500..15477530hg38UCSC Ensembl
chr9:15477498..15477528hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5553878
Supporting Variants
Samples
Known GenesPSIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17020611
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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