A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426497



Internal ID205430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:91556542..91565000hg38UCSC Ensembl
chrX:90811541..90819999hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg388459
hg198459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741433
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426497
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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