A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516156



Internal ID22574118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:33124219..33126406hg38UCSC Ensembl
chrX:33142336..33144523hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg382188
hg192188
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5969794
Supporting Variants
Samples
Known GenesDMD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516156
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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