A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736351



Internal ID20512299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25312522..25312850hg38UCSC Ensembl
chr18:22892486..22892814hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290905
Samples
Known GenesZNF521
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736351
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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