A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563958



Internal ID336883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47517951..47521796hg38UCSC Ensembl
chrX:47377350..47381195hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg383846
hg193846
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736801
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563958
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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