A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17513444



Internal ID22571399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42717190..42728116hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3810927
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849277
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17513444
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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