A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5427437



Internal ID206341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103554037..103571451hg38UCSC Ensembl
chrX:102808965..102826379hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3817415
hg1917415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741785
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5427437
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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