A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260606



Internal ID20469824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185128125..185129498hg38UCSC Ensembl
chr4:186049279..186050652hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg381374
hg191374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744187
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260606
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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