A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470802



Internal ID21128355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116502425..116515865hg38UCSC Ensembl
chr11:116373142..116386582hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3813441
hg1913441
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195588
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470802
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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