A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181505



Internal ID20748545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19207516..19227827hg38UCSC Ensembl
chr11:19229063..19249374hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3820312
hg1920312
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451422
Supporting Variants
Samples
Known GenesCSRP3, E2F8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181505
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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