A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191015



Internal ID20758055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2172083..2270940hg38UCSC Ensembl
chr11:2193313..2292170hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3898858
hg1998858
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446440
Supporting Variants
Samples
Known GenesASCL2, MIR4686
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191015
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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