A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464993



Internal ID21122546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65159793..65175552hg38UCSC Ensembl
chr11:64927264..64943023hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3815760
hg1915760
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196528
Samples
Known GenesSPDYC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464993
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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