A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6871806



Internal ID9921423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:161512738..161594513hg38UCSC Ensembl
Outerchr1:161482528..161564303hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3881776
hg1981776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718873
Supporting Variants
SamplesSSM091
Known GenesFCGR2A, FCGR2C, FCGR3A, HSPA6
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)essv6871806
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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