A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498312



Internal ID20871522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19886212..19897370hg38UCSC Ensembl
chr16:19897534..19908692hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3811159
hg1911159
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181033
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498312
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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