A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185837



Internal ID20752877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46457965..46815552hg38UCSC Ensembl
chr11:46479515..46837102hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38357588
hg19357588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473242
Supporting Variants
Samples
Known GenesAMBRA1, ARHGAP1, ATG13, CKAP5, F2, HARBI1, MIR5582, SNORD67, ZNF408
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185837
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer