A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513835



Internal ID20887183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6035407..6178599hg38UCSC Ensembl
chr16:6085408..6228600hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38143193
hg19143193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030516
Samples
Known GenesRBFOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513835
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