A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352111



Internal ID21009664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:28079534..28091433hg38UCSC Ensembl
chr2:28302401..28314300hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg3811900
hg1911900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087486
Samples
Known GenesBRE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352111
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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