A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178748



Internal ID20745788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65821424..65841587hg38UCSC Ensembl
chr11:65588895..65609058hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3820164
hg1920164
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471918
Supporting Variants
Samples
Known GenesSNX32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178748
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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