A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741937



Internal ID20517916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9398507..9398591hg38UCSC Ensembl
chr18:9398505..9398589hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275134
Samples
Known GenesTWSG1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741937
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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