A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363638



Internal ID21021191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38502175..38504605hg38UCSC Ensembl
chr3:38543666..38546096hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg382431
hg192431
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211198
Samples
Known GenesEXOG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363638
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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