A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5421211



Internal ID200294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56349303..56352959hg38UCSC Ensembl
chrX:56375736..56379392hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg383657
hg193657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv568n206
Supporting Variantsnssv17740248
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5421211
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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