A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658398



Internal ID9924503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161528729..161604404hg38UCSC Ensembl
Outerchr1:161528695..161604439hg38UCSC Ensembl
Innerchr1:161498519..161574194hg19UCSC Ensembl
Outerchr1:161498485..161574229hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3875745
hg1975745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv74e199
Supporting Variantsessv5918215
SamplesHG00359
Known GenesFCGR2C, FCGR3A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658398
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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