A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093488



Internal ID22002721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121958984..121958984hg38UCSC Ensembl
chr10:123718499..123718499hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586378
Samples
Known GenesNSMCE4A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093488
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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