A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17853573



Internal ID22037216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38715967..38715967hg38UCSC Ensembl
chr3:38757458..38757458hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6253894
Supporting Variants
Samples
Known GenesSCN10A
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17853573
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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