A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17858039



Internal ID22041682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163213673..163213673hg38UCSC Ensembl
chr6:163634705..163634705hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6260944
Supporting Variants
Samples
Known GenesPACRG
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17858039
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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