A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17858604



Internal ID22042247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:153095119..153095119hg38UCSC Ensembl
chr5:152474679..152474679hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6244990
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17858604
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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