A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093408



Internal ID22002641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96232271..96232271hg38UCSC Ensembl
chr10:97992027..97992027hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581084
Samples
Known GenesBLNK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093408
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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