A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18021616



Internal ID20588657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88855382..88864914hg38UCSC Ensembl
chr14:89321726..89331258hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg389533
hg199533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499677
Supporting Variants
Samples
Known GenesTTC8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18021616
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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