A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv421n223



Internal ID22803389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161591001..161629000hg38UCSC Ensembl
chr1:161560791..161598790hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3838000
hg1938000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6332081, nsv6330850, nsv6318862
Samples
Known GenesFCGR2C, FCGR3B, HSPA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv421n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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