A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393764



Internal ID21051317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153681401..153686700hg38UCSC Ensembl
chr4:154602553..154607852hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212117
Samples
Known GenesTLR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393764
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