A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457807



Internal ID21115360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:91312240..91402346hg38UCSC Ensembl
chr11:91045407..91135512hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3890107
hg1990106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995164
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457807
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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