A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16270651



Internal ID20479869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154460915..154460977hg38UCSC Ensembl
chrX:153689255..153689317hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752074
Supporting Variants
Samples
Known GenesPLXNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16270651
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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