A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463339



Internal ID21120892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44851597..44852080hg38UCSC Ensembl
chr11:44873148..44873631hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38484
hg19484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991671
Samples
Known GenesTSPAN18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463339
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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