A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749133



Internal ID20525162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:49080246..49080418hg38UCSC Ensembl
chr18:46606616..46606788hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272962
Samples
Known GenesDYM
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749133
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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