A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499855



Internal ID20873080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1948840..1970124hg38UCSC Ensembl
chr16:1998841..2020125hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3821285
hg1921285
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185801
Samples
Known GenesNDUFB10, RNF151, RPL3L, RPS2, SNHG9, SNORA10, SNORA64, SNORA78
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499855
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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