A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090235



Internal ID21999468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17867344..17867344hg38UCSC Ensembl
chr10:18156273..18156273hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589502
Samples
Known GenesMRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090235
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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