A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033835



Internal ID20600875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89829901..89830900hg38UCSC Ensembl
chr16:89896309..89897308hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496282
Supporting Variants
Samples
Known GenesSPIRE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033835
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02761


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