A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5428832



Internal ID207690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:10215967..10216035hg38UCSC Ensembl
chrX:10184007..10184075hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739217
Samples
Known GenesCLCN4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5428832
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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