A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361089



Internal ID21018642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87474432..87537377hg38UCSC Ensembl
chr3:87523582..87586527hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg3862946
hg1962946
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210172
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361089
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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