A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452707



Internal ID21110260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:486633..511168hg38UCSC Ensembl
chr11:486633..511168hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3824536
hg1924536
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190542
Samples
Known GenesPTDSS2, RNH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452707
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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