A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18030860



Internal ID20597900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58489107..58490998hg38UCSC Ensembl
chr16:58523011..58524902hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg381892
hg191892
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511280
Supporting Variants
Samples
Known GenesNDRG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18030860
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00044


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