A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854051



Internal ID22037694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:55321756..55321756hg38UCSC Ensembl
chr1:55787429..55787429hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6253483
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854051
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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