A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994243



Internal ID20561283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:79638801..79646500hg38UCSC Ensembl
chr11:79349845..79357544hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg387700
hg197700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467699
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994243
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