A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366952



Internal ID21024505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:35215401..35217600hg38UCSC Ensembl
chr3:35256893..35259092hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210557
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366952
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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