A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763088



Internal ID20538948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153382526..153382526hg38UCSC Ensembl
chrX:152647984..152647984hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381936
hg191936
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270675
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763088
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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