A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464128



Internal ID21121681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33126376..33419764hg38UCSC Ensembl
chr11:33147922..33441310hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38293389
hg19293389
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1020n223
Supporting Variantsnssv18189167
Samples
Known GenesCSTF3, CSTF3-AS1, HIPK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464128
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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