A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468839



Internal ID21126392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66021869..66023405hg38UCSC Ensembl
chr11:65789340..65790876hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381537
hg191537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992538
Samples
Known GenesCATSPER1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468839
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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