A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839335



Internal ID22022978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141013590..141013590hg38UCSC Ensembl
chr7:140713390..140713390hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6239845
Supporting Variants
Samples
Known GenesMRPS33
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839335
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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