A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450295



Internal ID21107848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28260302..28260686hg38UCSC Ensembl
chr11:28281849..28282233hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990134
Samples
Known GenesMETTL15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450295
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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