A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839209



Internal ID22022852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35112756..35112756hg38UCSC Ensembl
chr8:34970274..34970274hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6245874
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839209
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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