A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457779



Internal ID21115332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:91770801..91774400hg38UCSC Ensembl
chr11:91503967..91507566hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995311
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457779
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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