A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17640337



Internal ID21832384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154460912..154460975hg38UCSC Ensembl
chrX:153689252..153689315hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109177
Supporting Variants
Samples
Known GenesPLXNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17640337
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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