A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464386



Internal ID21121939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77569795..77724740hg38UCSC Ensembl
chr11:77280840..77435785hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38154946
hg19154946
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195264
Samples
Known GenesAQP11, CLNS1A, RSF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464386
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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