A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993135



Internal ID20560175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61333391..61339107hg38UCSC Ensembl
chr11:61100863..61106579hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg385717
hg195717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465452
Supporting Variants
Samples
Known GenesDAK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993135
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