A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094190



Internal ID20661230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132697698..132712076hg38UCSC Ensembl
chr3:132416542..132430920hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3814379
hg1914379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371675
Supporting Variants
Samples
Known GenesNPHP3, NPHP3-ACAD11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094190
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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