A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465847



Internal ID21123400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62818801..62820400hg38UCSC Ensembl
chr11:62586273..62587872hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993235
Samples
Known GenesSTX5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465847
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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