A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349783



Internal ID21007336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25634947..25706446hg38UCSC Ensembl
chr2:25857816..25929315hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3871500
hg1971500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209116
Samples
Known GenesDTNB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349783
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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