A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994940



Internal ID20561980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87324286..87325074hg38UCSC Ensembl
chr11:87035328..87036116hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38789
hg19789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474990
Supporting Variants
Samples
Known GenesTMEM135
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994940
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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