A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555468



Internal ID328624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:66961156..66966401hg38UCSC Ensembl
chrX:66180998..66186243hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg385246
hg195246
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740465
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555468
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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