A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17858805



Internal ID22042448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:165373305..165373305hg38UCSC Ensembl
chr5:164800311..164800311hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6256403
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17858805
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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