A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17990226



Internal ID20557267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29471001..29471800hg38UCSC Ensembl
chr11:29492548..29493347hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448648
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17990226
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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