A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465217



Internal ID22523106
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 Variantsnsv5881276
Supporting Variants
Samples
Known GenesDMD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465217
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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