A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431913



Internal ID22489783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:80862586..80862586hg38UCSC Ensembl
chr9:83477501..83477501hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5948777
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431913
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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