A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766963



Internal ID20542823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120784975..120784975hg38UCSC Ensembl
chrX:119918829..119918829hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38257
hg19257
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275391
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766963
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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