A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466732



Internal ID21124285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65019249..65022926hg38UCSC Ensembl
chr11:64786721..64790398hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg383678
hg193678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994082
Samples
Known GenesARL2, ARL2-SNX15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466732
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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