A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215539



Internal ID20782579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:129665120..129708432hg38UCSC Ensembl
chr6:129986265..130029577hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg3843313
hg1943313
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609656
Supporting Variants
Samples
Known GenesARHGAP18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215539
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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