A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757986



Internal ID20533846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52041520..52212575hg38UCSC Ensembl
chrX:51784616..51955702hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38171056
hg19171087
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286816
Samples
Known GenesMAGED4, MAGED4B, SNORA11D, SNORA11E
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757986
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer