A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393267



Internal ID21050820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38006518..38007292hg38UCSC Ensembl
chr4:38008139..38008913hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213552
Samples
Known GenesTBC1D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393267
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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