A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455668



Internal ID21113221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99068427..99098870hg38UCSC Ensembl
chr11:98939157..98969600hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3830444
hg1930444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996063
Samples
Known GenesCNTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455668
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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