A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974046



Internal ID22748981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149488859..149526566hg38UCSC Ensembl
chrX:148570390..148608105hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3837708
hg1937716
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447296
Samples
Known GenesIDS
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974046
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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