A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752392



Internal ID20528252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:72740927..72979902hg38UCSC Ensembl
chrX:71960751..72199738hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg38238976
hg19238988
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264636
Samples
Known GenesDMRTC1, DMRTC1B, FAM226A, FAM226B, LINC00684
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752392
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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