A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468772



Internal ID21126325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66034397..66037663hg38UCSC Ensembl
chr11:65801868..65805134hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg383267
hg193267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992539
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468772
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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