A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094283



Internal ID20661323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141062834..141062992hg38UCSC Ensembl
chr3:140781676..140781834hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371861
Supporting Variants
Samples
Known GenesSPSB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094283
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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