A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854149



Internal ID22037792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113465320..113465320hg38UCSC Ensembl
chr3:113184167..113184167hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6254531
Supporting Variants
Samples
Known GenesSPICE1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854149
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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