A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468780



Internal ID21126333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72136048..72172507hg38UCSC Ensembl
chr11:71847094..71883551hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3836460
hg1936458
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190147
Samples
Known GenesFOLR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468780
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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