A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5414917



Internal ID194182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:138015376..138016004hg38UCSC Ensembl
chrX:137097535..137098163hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742595
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5414917
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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