A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367779



Internal ID21025332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:118994301..119095100hg38UCSC Ensembl
chr3:118713148..118813947hg19UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg38100800
hg19100800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4989n223
Supporting Variantsnssv18207896
Samples
Known GenesIGSF11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367779
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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