A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472245



Internal ID21129798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76772442..76788251hg38UCSC Ensembl
chr11:76483486..76499295hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3815810
hg1915810
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181746
Samples
Known GenesTSKU
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472245
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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