A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167230



Internal ID21446235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:33190462..33190785hg38UCSC Ensembl
chrX:33208579..33208902hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5669534
Supporting Variants
SamplesHG00732
Known GenesDMD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167230
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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