A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5432550



Internal ID211288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:94232047..94233008hg38UCSC Ensembl
chrX:93487046..93488007hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg38962
hg19962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741520
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5432550
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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