A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083304



Internal ID21992537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69515445..69515445hg38UCSC Ensembl
chr10:71275201..71275201hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585568
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083304
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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