A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610880



Internal ID20983951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132173320..132194599hg38UCSC Ensembl
chr6:132494460..132515739hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3821280
hg1921280
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215576
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610880
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