A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465370



Internal ID21122923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76380101..76382300hg38UCSC Ensembl
chr11:76091145..76093344hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186942
Samples
Known GenesLOC100506127, PRKRIR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465370
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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