A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419529



Internal ID198659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:53108261..53111047hg38UCSC Ensembl
chrX:53137443..53140229hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg382787
hg192787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737022
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419529
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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