A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767002



Internal ID20542862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101598810..101614975hg38UCSC Ensembl
chrX:100853788..100869965hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3816166
hg1916178
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276193
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767002
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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