A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469282



Internal ID21126835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44959509..44966807hg38UCSC Ensembl
chr11:44981060..44988358hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg387299
hg197299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991675
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469282
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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