A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5430939



Internal ID209732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:64009213..64024279hg38UCSC Ensembl
chrX:63229093..63244159hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg3815067
hg1915067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740346
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5430939
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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