A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467454



Internal ID21125007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65314694..65328656hg38UCSC Ensembl
chr11:65082165..65096127hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3813963
hg1913963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1213n223
Supporting Variantsnssv17994104
Samples
Known GenesCDC42EP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467454
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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