A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618588



Internal ID20991659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:126497688..127079526hg38UCSC Ensembl
chr6:126818834..127400671hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg38581839
hg19581838
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215514
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618588
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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