A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17858010



Internal ID22041653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160748442..160748442hg38UCSC Ensembl
chr6:161169474..161169474hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6260916
Supporting Variants
Samples
Known GenesPLG
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17858010
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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