A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091787



Internal ID22001020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59646772..59646772hg38UCSC Ensembl
chr10:61406530..61406530hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578857
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091787
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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