A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456559



Internal ID21114112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93324201..93332900hg38UCSC Ensembl
chr11:93057367..93066066hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg388700
hg198700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1272n223
Supporting Variantsnssv18193569
Samples
Known GenesCCDC67
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456559
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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