A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056897



Internal ID21966132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206864617..206864617hg38UCSC Ensembl
chr1:207037962..207037962hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519355
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056897
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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