A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378794



Internal ID21036347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158049342..158252026hg38UCSC Ensembl
chr4:158970494..159173178hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38202685
hg19202685
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212747
Samples
Known GenesFAM198B, TMEM144
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378794
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