A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448957



Internal ID21106510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22643873..22652888hg38UCSC Ensembl
chr11:22665419..22674434hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg389016
hg199016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990194
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448957
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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