A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506186



Internal ID20879463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24632146..24648522hg38UCSC Ensembl
chr16:24643467..24659843hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3816377
hg1916377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506186
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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