A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3946175



Internal ID21366246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10764742..10764848hg38UCSC Ensembl
chr16:10858599..10858705hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15184185
SamplesHG002
Known GenesNUBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3946175
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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