A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361296



Internal ID21018849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:22506019..22783843hg38UCSC Ensembl
chr3:22547510..22825334hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38277825
hg19277825
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210410
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361296
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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