A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995389



Internal ID20562429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9249041..9251806hg38UCSC Ensembl
chr11:9270588..9273353hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382766
hg192766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448611
Supporting Variants
Samples
Known GenesDENND5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995389
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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