A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322926



Internal ID20856041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:239424361..239435218hg38UCSC Ensembl
chr1:239587661..239598518hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3810858
hg1910858
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202526
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322926
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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