A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5423433



Internal ID202454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:92891800..92952542hg38UCSC Ensembl
chrX:92146799..92207541hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg3860743
hg1960743
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741475
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5423433
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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