A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100659



Internal ID22009892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:129849679..129849785hg38UCSC Ensembl
chrX:128983655..128983761hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643928
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100659
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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