A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988207



Internal ID20555247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133855001..133858700hg38UCSC Ensembl
chr11:133724896..133728595hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465011
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988207
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00038


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