A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839620



Internal ID22023263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54432304..54432304hg38UCSC Ensembl
chr8:55344864..55344864hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6246004
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839620
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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