A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749747



Internal ID20525780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76392840..76393072hg38UCSC Ensembl
chr18:74104796..74105028hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274962
Samples
Known GenesZNF516
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749747
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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