A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097469



Internal ID20664509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169371901..169375100hg38UCSC Ensembl
chr3:169089689..169092888hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368819
Supporting Variants
Samples
Known GenesMECOM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097469
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00054


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