A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6258065



Internal ID22062675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205300975..205300975hg38UCSC Ensembl
chr1:205270103..205270103hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17842237
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6258065
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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