A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466122



Internal ID21123675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65006087..65024224hg38UCSC Ensembl
chr11:64773559..64791696hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3818138
hg1918138
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188146
Samples
Known GenesARL2, ARL2-SNX15, MIR6879
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466122
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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