A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671883



Internal ID21620190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52078072..52176358hg38UCSC Ensembl
chrX:51821168..51919454hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3898287
hg1998287
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167842
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671883
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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