A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563162



Internal ID336099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149487533..149527927hg38UCSC Ensembl
chrX:148569064..148609466hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3840395
hg1940403
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737904
Samples
Known GenesIDS, LINC00893
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563162
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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