A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766931



Internal ID20542791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:4265475..4265475hg38UCSC Ensembl
chr18:4265475..4265475hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293721
Samples
Known GenesDLGAP1, DLGAP1-AS5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766931
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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