A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17549755



Internal ID21874110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16094106..16094168hg38UCSC Ensembl
chr4:16095729..16095791hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5996226
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17549755
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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