A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012593



Internal ID21921936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130140698..130141166hg38UCSC Ensembl
chr10:131938962..131939430hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584586
Samples
Known GenesGLRX3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012593
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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