A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475395



Internal ID21132948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:104163006..105424222hg38UCSC Ensembl
chr11:104033734..105294949hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381261217
hg191261216
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191279
Samples
Known GenesCARD16, CARD17, CARD18, CASP1, CASP12, CASP4, CASP5, LOC643733, PDGFD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475395
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