A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071246



Internal ID21980479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169913435..169913435hg38UCSC Ensembl
chr4:170834586..170834586hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546480
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071246
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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