A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497385



Internal ID20870591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11869019..11881076hg38UCSC Ensembl
chr16:11962876..11974933hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3812058
hg1912058
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187765
Samples
Known GenesGSPT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497385
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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