A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5430943



Internal ID209736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155386103..155400400hg38UCSC Ensembl
chrX:154615752..154630061hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3814298
hg1914310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738202
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5430943
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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