A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973830



Internal ID22748765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:131841130..132003918hg38UCSC Ensembl
chrX:130975158..131137946hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg38162789
hg19162789
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442341
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973830
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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