A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997927



Internal ID21907270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67295805..67314750hg38UCSC Ensembl
chr4:68161523..68180468hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3818946
hg1918946
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537626
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997927
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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