A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463036



Internal ID22520921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:51536782..52222904hg38UCSC Ensembl
chrX:51279634..51966031hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38686123
hg19686398
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977584
Supporting Variants
Samples
Known GenesCENPVP1, CENPVP2, GSPT2, MAGED1, MAGED4, MAGED4B, SNORA11D, SNORA11E
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463036
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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