A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216682



Internal ID20783722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155541669..156975123hg38UCSC Ensembl
chr6:155862803..157296257hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg381433455
hg191433455
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609949
Supporting Variants
Samples
Known GenesARID1B, MIR4466
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216682
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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