A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216852



Internal ID20783892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137815526..137826302hg38UCSC Ensembl
chr6:138136663..138147439hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3810777
hg1910777
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610182
Supporting Variants
Samples
Known GenesLOC100130476
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216852
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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