A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201268



Internal ID20768308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161594185..161676042hg38UCSC Ensembl
chr1:161563975..161645832hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3881858
hg1981858
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6333854
Supporting Variants
Samples
Known GenesFCGR2B, FCGR2C, FCGR3B, HSPA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201268
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.07235


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