A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076405



Internal ID21985638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86493193..86493193hg38UCSC Ensembl
chr3:86542343..86542343hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552755
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076405
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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