A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998062



Internal ID21907405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70516302..70516405hg38UCSC Ensembl
chr4:71382019..71382122hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537811
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998062
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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