A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17852276



Internal ID22035919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:43126844..43126844hg38UCSC Ensembl
chr1:43592515..43592515hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6252782
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17852276
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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