A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876103



Internal ID22651063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:32069474..32078364hg38UCSC Ensembl
chrX:32087591..32096481hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg388891
hg198891
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453475
Samples
Known GenesDMD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876103
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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