A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617716



Internal ID20990787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:100227101..100230700hg38UCSC Ensembl
chr6:100674977..100678576hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215500
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617716
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer