A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470412



Internal ID21127965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74310401..74335900hg38UCSC Ensembl
chr11:74021446..74046945hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3825500
hg1925500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1229n223
Supporting Variantsnssv18195575
Samples
Known GenesP4HA3, PGM2L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470412
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