A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329666



Internal ID20862819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158531793..158545609hg38UCSC Ensembl
chr1:158501583..158515399hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3813817
hg1913817
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329666
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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