A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514150



Internal ID20887502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81765053..81772726hg38UCSC Ensembl
chr16:81798658..81806331hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg387674
hg197674
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184400
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514150
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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