A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449089



Internal ID21106642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4393001..4394600hg38UCSC Ensembl
chr11:4414231..4415830hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991382
Samples
Known GenesTRIM21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449089
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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