A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455730



Internal ID21113283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84291354..84425805hg38UCSC Ensembl
chr11:84002397..84136848hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38134452
hg19134452
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182474
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455730
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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