A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215568



Internal ID20782608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131789241..131944175hg38UCSC Ensembl
chr6:132110381..132265315hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38154935
hg19154935
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611969
Supporting Variants
Samples
Known GenesENPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215568
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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