A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17513702



Internal ID22571658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5330288..5337321hg38UCSC Ensembl
chr9:5330288..5337321hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg387034
hg197034
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855547
Supporting Variants
Samples
Known GenesRLN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17513702
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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