A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191628



Internal ID20758668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63925132..63926190hg38UCSC Ensembl
chr11:63692604..63693662hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381059
hg191059
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475029
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191628
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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