A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328110



Internal ID20861255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32935327..32939395hg38UCSC Ensembl
chr1:33400928..33404996hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg384069
hg194069
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203615
Samples
Known GenesRNF19B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328110
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer