A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190994



Internal ID20758034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56574953..56582708hg38UCSC Ensembl
chr11:56342429..56350184hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg387756
hg197756
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6470235
Supporting Variants
Samples
Known GenesOR5M10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190994
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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