A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv402n223



Internal ID22803370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161511475..161615542hg38UCSC Ensembl
chr1:161481265..161585332hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38104068
hg19104068
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6334910, nsv6332311, nsv6329914, nsv6335401, nsv6323219
Samples
Known GenesFCGR2A, FCGR2C, FCGR3A, HSPA6, HSPA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv402n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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