A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461689



Internal ID21119242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46607086..46610480hg38UCSC Ensembl
chr11:46628636..46632030hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg383395
hg193395
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187640
Samples
Known GenesHARBI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461689
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