A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457728



Internal ID21115281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65036707..65039037hg38UCSC Ensembl
chr11:64804179..64806509hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382331
hg192331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994084
Samples
Known GenesARL2-SNX15, SNX15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457728
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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