A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496218



Internal ID20869417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89346802..89674039hg38UCSC Ensembl
chr16:89413210..89740447hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38327238
hg19327238
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180274
Samples
Known GenesANKRD11, CHMP1A, CPNE7, DPEP1, RPL13, SNORD68, SPATA33, SPG7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496218
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