A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749567



Internal ID20525599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6299706..6299784hg38UCSC Ensembl
chr4:6301433..6301511hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280369
Samples
Known GenesWFS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749567
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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