A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093957



Internal ID22003190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121100303..121100303hg38UCSC Ensembl
chr10:122859817..122859817hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588428
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093957
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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