A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17512362



Internal ID22570315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:24377940..24380139hg38UCSC Ensembl
chr9:24377938..24380137hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863144
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17512362
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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