A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17857283



Internal ID22040926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101096447..101096447hg38UCSC Ensembl
chr1:101562003..101562003hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6256235
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17857283
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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