A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074059



Internal ID21983292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43965608..43965608hg38UCSC Ensembl
chr7:44005207..44005207hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564503
Samples
Known GenesPOLR2J4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074059
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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