A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843626



Internal ID22027269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:16510979..16510979hg38UCSC Ensembl
chr12:16663913..16663913hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6240704
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843626
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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