A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5552358



Internal ID325728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15611186..15669107hg38UCSC Ensembl
chrX:15629309..15687230hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3857922
hg1957922
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739405
Samples
Known GenesTMEM27
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5552358
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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