A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3946945



Internal ID21367015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6977649..6977729hg38UCSC Ensembl
chr4:6979376..6979456hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15180026
SamplesHG002
Known GenesTBC1D14
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3946945
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