A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061509



Internal ID21970742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163110329..163110329hg38UCSC Ensembl
chr4:164031481..164031481hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549846
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061509
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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