A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450936



Internal ID21108489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3394935..3594137hg38UCSC Ensembl
chr11:3416165..3615367hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38199203
hg19199203
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188716
Samples
Known GenesLOC650368
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450936
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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