A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508770



Internal ID20882074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:53878699..53897787hg38UCSC Ensembl
chr16:53912611..53931699hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3819089
hg1919089
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194690
Samples
Known GenesFTO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508770
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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