A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470936



Internal ID21128489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42603266..42603788hg38UCSC Ensembl
chr11:42624816..42625338hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38523
hg19523
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991285
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470936
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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