A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5433474



Internal ID212187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140520963..140521944hg38UCSC Ensembl
chrX:139603128..139604109hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38982
hg19982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742695
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5433474
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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