A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969074



Internal ID22744009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:84879978..84910969hg38UCSC Ensembl
chrX:84134984..84165975hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3830992
hg1930992
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464631
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969074
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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