A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746359



Internal ID20522371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103772854..103772854hg38UCSC Ensembl
chrX:103027782..103027782hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg383330
hg193330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262183
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746359
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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