A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854865



Internal ID22038508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59946844..59946844hg38UCSC Ensembl
chr1:60412516..60412516hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6253863
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854865
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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