A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449116



Internal ID21106669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28295341..28295798hg38UCSC Ensembl
chr11:28316888..28317345hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38458
hg19458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990141
Samples
Known GenesMETTL15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449116
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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