A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178997



Internal ID20746037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9181561..9299354hg38UCSC Ensembl
chr11:9203108..9320901hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38117794
hg19117794
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443359
Supporting Variants
Samples
Known GenesDENND5A, TMEM41B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178997
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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