A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17848011



Internal ID22031654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88660317..88660317hg38UCSC Ensembl
chr16:88726725..88726725hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38249
hg19249
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6250526
Supporting Variants
Samples
Known GenesMVD
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17848011
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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