A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503856



Internal ID20877113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69207410..69220412hg38UCSC Ensembl
chr16:69241313..69254315hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3813003
hg1913003
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195115
Samples
Known GenesSNTB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503856
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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