A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319311



Internal ID20852405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240664829..240666442hg38UCSC Ensembl
chr1:240828129..240829742hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg381614
hg191614
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200605
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319311
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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