A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467536



Internal ID21125089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35222308..35237978hg38UCSC Ensembl
chr11:35243855..35259525hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3815671
hg1915671
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190101
Samples
Known GenesCD44
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467536
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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