A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558381



Internal ID331446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26782003..26803637hg38UCSC Ensembl
chrX:26800120..26821754hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3821635
hg1921635
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736262
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558381
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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