A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078281



Internal ID21987514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165598021..165598021hg38UCSC Ensembl
chr4:166519173..166519173hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551882
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078281
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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