A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555995



Internal ID329142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:131678316..131841115hg38UCSC Ensembl
chrX:130812329..130975143hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg38162800
hg19162815
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737619
Samples
Known GenesLOC286467
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555995
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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