A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745392



Internal ID20521400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:33096312..33096369hg38UCSC Ensembl
chr18:30676276..30676333hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278613
Samples
Known GenesCCDC178
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745392
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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