A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180685



Internal ID20747725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:5322186..5985865hg38UCSC Ensembl
chr16:5372187..6035866hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38663680
hg19663680
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510004
Supporting Variants
Samples
Known GenesMIR8065
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180685
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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