A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739914



Internal ID163580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:32702967..32792243hg38UCSC Ensembl
chrX:32721084..32810360hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3889277
hg1989277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5418696
Supporting Variants
Samples
Known GenesDMD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739914
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0031224


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