A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987961



Internal ID20555001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131838055..131838599hg38UCSC Ensembl
chr11:131707949..131708493hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38545
hg19545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464163
Supporting Variants
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987961
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00049


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