A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458984



Internal ID21116537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57784060..57790244hg38UCSC Ensembl
chr11:57551532..57557716hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg386185
hg196185
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183035
Samples
Known GenesCTNND1, TMX2-CTNND1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458984
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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