A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3947550



Internal ID21367619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152719149..152719486hg38UCSC Ensembl
chrX:151887638..151887975hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15200434
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3947550
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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