A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969898



Internal ID22744833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:32066555..32076122hg38UCSC Ensembl
chrX:32084672..32094239hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg389568
hg199568
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516141
Samples
Known GenesDMD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969898
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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