A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18030151



Internal ID20597191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:54766401..54775300hg38UCSC Ensembl
chr16:54800313..54809212hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg388900
hg198900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499101
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18030151
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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