A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184499



Internal ID20751539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64261568..64274442hg38UCSC Ensembl
chr11:64029040..64041914hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3812875
hg1912875
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465257
Supporting Variants
Samples
Known GenesBAD, PLCB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184499
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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