A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17841159



Internal ID22024802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35633589..35633589hg38UCSC Ensembl
chr9:35633586..35633586hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6257604
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17841159
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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