A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398086



Internal ID21055639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13282921..13284682hg38UCSC Ensembl
chr6:13283153..13284914hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg381762
hg191762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140317
Samples
Known GenesLOC100130357, PHACTR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398086
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