A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068847



Internal ID21978080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88994240..88994240hg38UCSC Ensembl
chr5:88290057..88290057hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546892
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068847
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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