A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437883



Internal ID21095436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13775331..13848416hg38UCSC Ensembl
chr11:13796878..13869963hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3873086
hg1973086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988293
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437883
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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