A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739444



Internal ID163110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:16676560..16677107hg38UCSC Ensembl
chrX:16694683..16695230hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38548
hg19548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433196
Supporting Variants
Samples
Known GenesCTPS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739444
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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