A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457681



Internal ID21115234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99155801..99157700hg38UCSC Ensembl
chr11:99026532..99028431hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996080
Samples
Known GenesCNTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457681
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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