A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745185



Internal ID20521190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9385391..9385720hg38UCSC Ensembl
chr18:9385389..9385718hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265881
Samples
Known GenesTWSG1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745185
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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