A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109006



Internal ID22018239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:33190462..33190786hg38UCSC Ensembl
chrX:33208579..33208903hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644359
Samples
Known GenesDMD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109006
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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