A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447502



Internal ID21105055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:21042929..21443675hg38UCSC Ensembl
chr11:21064475..21465221hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38400747
hg19400747
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182305
Samples
Known GenesNELL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447502
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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