A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354116



Internal ID21011669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65079806..65080946hg38UCSC Ensembl
chr2:65306940..65308080hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg381141
hg191141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089331
Samples
Known GenesCEP68
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354116
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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