A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435849



Internal ID21093402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8776585..8790122hg38UCSC Ensembl
chr11:8798132..8811669hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3813538
hg1913538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994977
Samples
Known GenesST5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435849
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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