A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503237



Internal ID20876490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56457943..56465265hg38UCSC Ensembl
chr16:56491855..56499177hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg387323
hg197323
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193046
Samples
Known GenesOGFOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503237
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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