A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276579



Internal ID20485797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146104171..146104236hg38UCSC Ensembl
chr4:147025323..147025388hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733336
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276579
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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