A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365264



Internal ID21022817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77165001..77168900hg38UCSC Ensembl
chr3:77214152..77218051hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209387
Samples
Known GenesROBO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365264
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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