A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839219



Internal ID22022862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37077029..37077029hg38UCSC Ensembl
chr8:36934547..36934547hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6245885
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839219
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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