A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467058



Internal ID21124611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:2856497..2879312hg38UCSC Ensembl
chr12:2965663..2988478hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3822816
hg1922816
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193666
Samples
Known GenesFOXM1, LOC100507424, RHNO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467058
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