A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5420481



Internal ID199583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:84741900..84742029hg38UCSC Ensembl
chrX:83996908..83997037hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741150
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5420481
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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