A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17513000



Internal ID22570955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3471136..3473765hg38UCSC Ensembl
chr9:3471136..3473765hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg382630
hg192630
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858711
Supporting Variants
Samples
Known GenesRFX3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17513000
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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