A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457366



Internal ID21114919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117176601..117223100hg38UCSC Ensembl
chr11:117047317..117093816hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3846500
hg1946500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182968
Samples
Known GenesLOC100652768, PAFAH1B2, PCSK7, SIDT2, TAGLN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457366
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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