A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369390



Internal ID21026943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77149354..77171591hg38UCSC Ensembl
chr3:77198505..77220742hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3822238
hg1922238
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209386
Samples
Known GenesROBO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369390
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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