A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078953



Internal ID21988186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149654842..149654842hg38UCSC Ensembl
chr5:149034405..149034405hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg381816
hg191816
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078953
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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