A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975478



Internal ID22750413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151491627..151498350hg38UCSC Ensembl
chrX:150660099..150666822hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg386724
hg196724
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435941
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975478
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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