A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190131



Internal ID20757171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134221901..134225500hg38UCSC Ensembl
chr11:134091795..134095394hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472171
Supporting Variants
Samples
Known GenesNCAPD3, VPS26B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190131
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