A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17850760



Internal ID22034403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38654835..38654835hg38UCSC Ensembl
chr1:39120507..39120507hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6251915
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17850760
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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