A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766421



Internal ID20542281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:65369796..65373269hg38UCSC Ensembl
chrX:64589676..64593149hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg383474
hg193474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288744
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766421
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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