A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372087



Internal ID21029640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86737222..86884408hg38UCSC Ensembl
chr3:86786372..86933558hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38147187
hg19147187
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210145
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372087
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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