A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670711



Internal ID9590130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161620611..161628159hg38UCSC Ensembl
Outerchr1:161620574..161628209hg38UCSC Ensembl
Innerchr1:161590401..161597949hg19UCSC Ensembl
Outerchr1:161590364..161597999hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg387636
hg197636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6381464
SamplesNA18596
Known GenesFCGR3B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670711
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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