A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973845



Internal ID22748780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:117590518..117592205hg38UCSC Ensembl
chrX:116724481..116726168hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg381688
hg191688
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448966
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973845
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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