A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998400



Internal ID21907743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87534924..87570663hg38UCSC Ensembl
chr4:88456076..88491815hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3835740
hg1935740
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554864
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998400
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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