A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740383



Internal ID20516358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24023938..24023993hg38UCSC Ensembl
chr18:21603902..21603957hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274502
Samples
Known GenesTTC39C
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740383
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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