A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560364



Internal ID333373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:125098630..125102451hg38UCSC Ensembl
chrX:124232479..124236300hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg383822
hg193822
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742228
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560364
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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