A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978084



Internal ID22753019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52461893..52798149hg38UCSC Ensembl
chrX:52205036..52827189hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38336257
hg19622154
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454520
Samples
Known GenesSPANXN5, SSX2, SSX2B, SSX7, SSX8, XAGE1A, XAGE1B, XAGE1C, XAGE1D, XAGE1E, XAGE2, XAGE2B
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978084
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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