A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469340



Internal ID21126893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65603701..65605000hg38UCSC Ensembl
chr11:65371172..65372471hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178694
Samples
Known GenesMAP3K11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469340
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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