A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056425



Internal ID21965658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3693960..3693960hg38UCSC Ensembl
chr1:3610524..3610524hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536581
Samples
Known GenesTP73
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056425
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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