A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17513478



Internal ID22571433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42796692..42816561hg38UCSC Ensembl
chr9:44154558..44174427hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3819870
hg1919870
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867036
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17513478
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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