A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353747



Internal ID21011300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:123233139..123268697hg38UCSC Ensembl
chr2:123990715..124026273hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3835559
hg1935559
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207578
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353747
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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