A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216926



Internal ID20783966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143601596..143692510hg38UCSC Ensembl
chr6:143922733..144013647hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3890915
hg1990915
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603490
Supporting Variants
Samples
Known GenesPHACTR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216926
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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