A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16289959



Internal ID20499177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:32246198..32248172hg38UCSC Ensembl
chrX:32264315..32266289hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg381975
hg191975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767602
Supporting Variants
Samples
Known GenesDMD
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16289959
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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