A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616986



Internal ID20990057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154968822..154987899hg38UCSC Ensembl
chr6:155289956..155309033hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3819078
hg1919078
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216672
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616986
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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