A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470547



Internal ID21128100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66536655..66540511hg38UCSC Ensembl
chr11:66304126..66307982hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg383857
hg193857
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183875
Samples
Known GenesZDHHC24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470547
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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