A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444415



Internal ID21101968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16668211..16674788hg38UCSC Ensembl
chr11:16689758..16696335hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg386578
hg196578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988525
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444415
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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