A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741448



Internal ID165114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:92112160..92113796hg38UCSC Ensembl
chrX:91367159..91368795hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg381637
hg191637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138602
Supporting Variants
Samples
Known GenesPCDH11X
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741448
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.029943


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