A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437265



Internal ID21094818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17311552..17311909hg38UCSC Ensembl
chr11:17333099..17333456hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185353
Samples
Known GenesNUCB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437265
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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