A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6381464



Internal ID9358867
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 Flag1
Merged StatusS
Merged Variantsesv2670711
Supporting Variants
SamplesNA18596
Known GenesFCGR3B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6381464
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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