A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456154



Internal ID21113707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68988010..69010421hg38UCSC Ensembl
chr11:68755478..68777889hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3822412
hg1922412
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190380
Samples
Known GenesMRGPRF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456154
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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