A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970991



Internal ID22745926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:98429212..98556904hg38UCSC Ensembl
chrX:97684210..97811902hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38127693
hg19127693
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466222
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970991
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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