A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467948



Internal ID21125501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72070769..72084018hg38UCSC Ensembl
chr11:71781815..71795064hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3813250
hg1913250
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194906
Samples
Known GenesLRTOMT, MIR3165, NUMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467948
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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