A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17990241



Internal ID20557282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29554583..29554644hg38UCSC Ensembl
chr11:29576130..29576191hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453435
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17990241
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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