A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190837



Internal ID20757877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121289701..121293700hg38UCSC Ensembl
chr11:121160410..121164409hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461852
Supporting Variants
Samples
Known GenesSC5D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190837
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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