A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6871807



Internal ID9921424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:161558362..161639783hg38UCSC Ensembl
Outerchr1:161528152..161609573hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3881422
hg1981422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718884
Supporting Variants
SamplesSSM091
Known GenesFCGR2C, FCGR3B, HSPA7
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)essv6871807
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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