A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737746



Internal ID161412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:145217560..145271950hg38UCSC Ensembl
chrX:144299080..144353470hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3854391
hg1954391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425666
Supporting Variants
Samples
Known GenesSPANXN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737746
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00291363


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