A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17555947



Internal ID21880302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:58189924..58191217hg38UCSC Ensembl
chr4:59056090..59057383hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381294
hg191294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5997821
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17555947
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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