A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511253



Internal ID20884580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:60350260..60372291hg38UCSC Ensembl
chr16:60384164..60406195hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3822032
hg1922032
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189802
Samples
Known GenesLOC729159
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511253
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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