A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502383



Internal ID20875627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:60132580..60194513hg38UCSC Ensembl
chr16:60166484..60228417hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3861934
hg1961934
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191454
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502383
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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