A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987936



Internal ID20554976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131704897..131705517hg38UCSC Ensembl
chr11:131574791..131575411hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457893
Supporting Variants
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987936
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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