A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215566



Internal ID20782606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131739283..131739971hg38UCSC Ensembl
chr6:132060423..132061111hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38689
hg19689
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614339
Supporting Variants
Samples
Known GenesENPP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215566
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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