A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431343



Internal ID21088896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128470459..128522579hg38UCSC Ensembl
chr7:128110513..128162633hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3852121
hg1952121
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221373
Samples
Known GenesMETTL2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431343
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