A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5432824



Internal ID211557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:68785447..68785626hg38UCSC Ensembl
chrX:68005290..68005469hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740554
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5432824
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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