A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5428851



Internal ID207709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54318287..54318593hg38UCSC Ensembl
chrX:54344720..54345026hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740143
Samples
Known GenesWNK3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5428851
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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