A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033931



Internal ID20600971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15674170..15690534hg38UCSC Ensembl
chr17:15577484..15593848hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3816365
hg1916365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510825
Supporting Variants
Samples
Known GenesTRIM16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033931
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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