A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17852105



Internal ID22035748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42787595..42787595hg38UCSC Ensembl
chr3:42829087..42829087hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6253933
Supporting Variants
Samples
Known GenesHIGD1A
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17852105
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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