A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843763



Internal ID22027406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:213014276..213014276hg38UCSC Ensembl
chr1:213187618..213187618hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6258128
Supporting Variants
Samples
Known GenesANGEL2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843763
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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