A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17844250



Internal ID22027893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:236656976..236656976hg38UCSC Ensembl
chr1:236820276..236820276hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6241342
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17844250
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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