A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458774



Internal ID21116327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90868561..90869172hg38UCSC Ensembl
chr11:90601729..90602340hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995100
Samples
Known GenesDISC1FP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458774
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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