A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17849306



Internal ID22032949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:39513534..39513534hg38UCSC Ensembl
chr18:37093498..37093498hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6242319
Supporting Variants
Samples
Known GenesLINC00669
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17849306
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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