A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512328



Internal ID20885661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67787162..67802501hg38UCSC Ensembl
chr16:67821065..67836404hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3815340
hg1915340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030831
Samples
Known GenesRANBP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512328
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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