A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465634



Internal ID21123187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72355538..72356037hg38UCSC Ensembl
chr11:72066582..72067081hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187871
Samples
Known GenesCLPB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465634
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