A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437985



Internal ID21095538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17009239..17013154hg38UCSC Ensembl
chr11:17030786..17034701hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg383916
hg193916
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180299
Samples
Known GenesPLEKHA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437985
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