A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082124



Internal ID21991357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124052991..124052991hg38UCSC Ensembl
chr10:125812507..125812507hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589062
Samples
Known GenesCHST15
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082124
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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