A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15200366



Internal ID21339181
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3936538
Supporting Variants
SamplesHG002
Known GenesDMD
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15200366
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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