A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17857997



Internal ID22041640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158868976..158868976hg38UCSC Ensembl
chr6:159290008..159290008hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6260903
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17857997
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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