A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453577



Internal ID21111130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17666818..17667673hg38UCSC Ensembl
chr11:17688365..17689220hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38856
hg19856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988608
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453577
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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