A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046405



Internal ID21955649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9872182..9872182hg38UCSC Ensembl
chr3:9913866..9913866hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535530
Samples
Known GenesCIDEC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046405
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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