A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167195



Internal ID21482920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:32373145..32373460hg38UCSC Ensembl
chrX:32391262..32391577hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670896
Supporting Variants
SamplesHG03732
Known GenesDMD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167195
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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