A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18053260



Internal ID20620300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161512746..161594464hg38UCSC Ensembl
chr1:161482536..161564254hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3881719
hg1981719
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332311
Supporting Variants
Samples
Known GenesFCGR2A, FCGR2C, FCGR3A, HSPA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18053260
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00802


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