A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17841081



Internal ID22024724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96277676..96277676hg38UCSC Ensembl
chr9:99039958..99039958hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6257932
Supporting Variants
Samples
Known GenesHSD17B3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17841081
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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