A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473154



Internal ID21130707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66010363..66013631hg38UCSC Ensembl
chr11:65777834..65781102hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg383269
hg193269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992537
Samples
Known GenesCST6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473154
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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