A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422003



Internal ID201058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:53180970..53182031hg38UCSC Ensembl
chrX:53210152..53211213hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg381062
hg191062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737024
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422003
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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