A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738090



Internal ID161756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153769676..153769746hg38UCSC Ensembl
chrX:153035131..153035201hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414144
Supporting Variants
Samples
Known GenesPLXNB3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738090
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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