A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463693



Internal ID21121246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47609281..47610503hg38UCSC Ensembl
chr11:47630833..47632055hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381223
hg191223
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463693
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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