A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739755



Internal ID20515730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54534021..54534021hg38UCSC Ensembl
chrX:54560454..54560454hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg381898
hg191898
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279706
Samples
Known GenesGNL3L
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739755
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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