A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994563



Internal ID20561603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81675775..81791235hg38UCSC Ensembl
chr11:81386817..81502277hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38115461
hg19115461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467279
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994563
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