A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027709



Internal ID20594749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99218111..99218591hg38UCSC Ensembl
chr15:99758316..99758796hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502316
Supporting Variants
Samples
Known GenesTTC23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027709
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00081


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