A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854807



Internal ID22038450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58777516..58777516hg38UCSC Ensembl
chr1:59243188..59243188hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6253760
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854807
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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