A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027566



Internal ID20594606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98433117..99147026hg38UCSC Ensembl
chr15:98976346..99687231hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38713910
hg19710886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504865
Supporting Variants
Samples
Known GenesFAM169B, IGF1R, MIR4714, PGPEP1L, SYNM, TTC23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027566
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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