A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5431032



Internal ID209820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:109020127..109031109hg38UCSC Ensembl
chrX:108263357..108274339hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3810983
hg1910983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741910
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5431032
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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