A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191607



Internal ID20758647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:24400001..24434100hg38UCSC Ensembl
chr11:24421547..24455646hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3834100
hg1934100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454853
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191607
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00016


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