A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339847



Internal ID20997400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26701736..26708470hg38UCSC Ensembl
chr2:26924604..26931338hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg386735
hg196735
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209131
Samples
Known GenesKCNK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339847
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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