A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399988



Internal ID21057541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12828359..12829677hg38UCSC Ensembl
chr6:12828591..12829909hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg381319
hg191319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137727
Samples
Known GenesPHACTR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399988
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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