A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752282



Internal ID20528142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52077120..52176972hg38UCSC Ensembl
chrX:51820216..51920068hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3899853
hg1999853
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261335
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752282
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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