A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17852122



Internal ID22035765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45638027..45638027hg38UCSC Ensembl
chr3:45679519..45679519hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6253952
Supporting Variants
Samples
Known GenesLIMD1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17852122
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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