A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453188



Internal ID21110741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7540405..7638699hg38UCSC Ensembl
chr11:7561636..7659930hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3898295
hg1998295
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181640
Samples
Known GenesPPFIBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453188
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