A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507555



Internal ID20880848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28265748..28318656hg38UCSC Ensembl
chr16:28277069..28329977hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3852909
hg1952909
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189760
Samples
Known GenesSBK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507555
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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