A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091422



Internal ID22000655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103909390..103909390hg38UCSC Ensembl
chr10:105669148..105669148hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580881
Samples
Known GenesOBFC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091422
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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