A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342136



Internal ID20999689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10466675..10479704hg38UCSC Ensembl
chr2:10606801..10619830hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3813030
hg1913030
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205807
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342136
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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