A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098850



Internal ID22008083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128186226..128186226hg38UCSC Ensembl
chr10:129984490..129984490hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg382126
hg192126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578187
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098850
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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