A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17858284



Internal ID22041927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:134067449..134067449hg38UCSC Ensembl
chr5:133403140..133403140hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6244862
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17858284
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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