A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17858084



Internal ID22041727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169461800..169461800hg38UCSC Ensembl
chr6:169861895..169861895hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6260989
Supporting Variants
Samples
Known GenesWDR27
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17858084
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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