A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936538



Internal ID21356607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:33190462..33190786hg38UCSC Ensembl
chrX:33208579..33208903hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15200366
SamplesHG002
Known GenesDMD
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936538
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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