A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026220



Internal ID85217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110974552..110996552hg38UCSC Ensembl
chr9:113736832..113758832hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3822001
hg1922001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493617
Supporting Variants
Samples
Known GenesLPAR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026220
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625


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