A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839859



Internal ID22023502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17190698..17190698hg38UCSC Ensembl
chr8:17048207..17048207hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6245700
Supporting Variants
Samples
Known GenesZDHHC2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839859
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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