A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465882



Internal ID21123435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90867111..90895644hg38UCSC Ensembl
chr11:90600279..90628812hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3828534
hg1928534
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180837
Samples
Known GenesDISC1FP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465882
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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