A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505399



Internal ID20878668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27307149..27312855hg38UCSC Ensembl
chr16:27318470..27324176hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg385707
hg195707
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184384
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505399
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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