A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18098227



Internal ID20665267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172961083..172973489hg38UCSC Ensembl
chr3:172678873..172691279hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3812407
hg1912407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356892
Supporting Variants
Samples
Known GenesSPATA16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18098227
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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