A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5414018



Internal ID193305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:125203000..125203085hg38UCSC Ensembl
chrX:124336849..124336934hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742234
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5414018
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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