A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17840140



Internal ID22023783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96397642..96397642hg38UCSC Ensembl
chr8:97409870..97409870hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6246356
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17840140
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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