A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17857342



Internal ID22040985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71390805..71390805hg38UCSC Ensembl
chr6:72100508..72100508hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6260831
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17857342
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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