A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739894



Internal ID163560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:32412261..32413519hg38UCSC Ensembl
chrX:32430378..32431636hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg381259
hg191259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415126
Supporting Variants
Samples
Known GenesDMD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739894
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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