A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371891



Internal ID21029444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:79188698..79199945hg38UCSC Ensembl
chr3:79237848..79249095hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3811248
hg1911248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104554
Samples
Known GenesROBO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371891
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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