A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093341



Internal ID22002574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91384445..91384445hg38UCSC Ensembl
chr10:93144202..93144202hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583038
Samples
Known GenesLOC100188947
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093341
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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