A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980083



Internal ID22755018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:25259004..25281867hg38UCSC Ensembl
chrX:25277121..25299984hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3822864
hg1922864
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466826
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5980083
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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