A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5430944



Internal ID209737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1668896..1669193hg38UCSC Ensembl
chrX:1787789..1788086hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738891
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5430944
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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