A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609920



Internal ID20982991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:118268441..118858796hg38UCSC Ensembl
chr6:118589604..119179959hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38590356
hg19590356
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214545
Samples
Known GenesBRD7P3, CEP85L, LOC100287632, MCM9, PLN, SLC35F1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609920
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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