A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074994



Internal ID21984227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184314977..184314977hg38UCSC Ensembl
chr4:185236130..185236130hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556329
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074994
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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