A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077408



Internal ID21986641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:102044514..102044514hg38UCSC Ensembl
chr3:101763358..101763358hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38964
hg19964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543366
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077408
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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