A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459310



Internal ID21116863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56836197..56855408hg38UCSC Ensembl
chr11:56603673..56622884hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3819212
hg1919212
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187888
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459310
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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