A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050697



Internal ID21959930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:31284589..31284589hg38UCSC Ensembl
chrX:31302706..31302706hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642994
Samples
Known GenesDMD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050697
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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