A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737992



Internal ID161658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151570543..151570931hg38UCSC Ensembl
chrX:150739015..150739403hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426290
Supporting Variants
Samples
Known GenesPASD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737992
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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