A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18028644



Internal ID20595684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11819761..11820877hg38UCSC Ensembl
chr16:11913618..11914734hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg381117
hg191117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498063
Supporting Variants
Samples
Known GenesBCAR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18028644
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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