A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046827



Internal ID21956060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:31284576..31284576hg38UCSC Ensembl
chrX:31302693..31302693hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643978
Samples
Known GenesDMD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046827
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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