A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355080



Internal ID21012633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:112340909..112348953hg38UCSC Ensembl
chr2:113098486..113106530hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg388045
hg198045
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206482
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355080
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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