A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17850738



Internal ID22034381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:34291997..34291997hg38UCSC Ensembl
chr21:35664297..35664297hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6251862
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17850738
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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