A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765890



Internal ID20541750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155075293..155075293hg38UCSC Ensembl
chrX:154303568..154303568hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286065
Samples
Known GenesBRCC3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765890
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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