A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063084



Internal ID21972317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156203194..156203194hg38UCSC Ensembl
chr4:157124346..157124346hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538325
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063084
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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