A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516155



Internal ID22574117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:33115573..33124218hg38UCSC Ensembl
chrX:33133690..33142335hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg388646
hg198646
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973713
Supporting Variants
Samples
Known GenesDMD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516155
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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