A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881880



Internal ID22656856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:33119067..33167375hg38UCSC Ensembl
chrX:33137184..33185492hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3848309
hg1948309
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453509
Samples
Known GenesDMD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881880
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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