A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342185



Internal ID20999738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25785397..25786413hg38UCSC Ensembl
chr2:26008266..26009282hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg381017
hg191017
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209119
Samples
Known GenesASXL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342185
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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