A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17847771



Internal ID22031414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74637145..74637145hg38UCSC Ensembl
chr16:74671043..74671043hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6250432
Supporting Variants
Samples
Known GenesRFWD3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17847771
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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