A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514207



Internal ID20887559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31553087..31572430hg38UCSC Ensembl
chr16:31564408..31583751hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3819344
hg1919344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028956
Samples
Known GenesYBX3P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514207
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