A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515062



Internal ID20888419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:73560701..73834943hg38UCSC Ensembl
chr16:73594600..73868842hg19UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg38274243
hg19274243
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177146
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515062
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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