A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457400



Internal ID21114953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60197701..60204300hg38UCSC Ensembl
chr11:59965174..59971773hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178283
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457400
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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