A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515167



Internal ID20888526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26359701..26374263hg38UCSC Ensembl
chr16:26371022..26385584hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3814563
hg1914563
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189009
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515167
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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