A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609660



Internal ID20982731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110866005..110869374hg38UCSC Ensembl
chr6:111187208..111190577hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg383370
hg193370
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216808
Samples
Known GenesAMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609660
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