A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6679918



Internal ID9749538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:42903173..42903835hg38UCSC Ensembl
Outerchr4:42905190..42905852hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2727494
Supporting Variants
SamplesSSM033
Known GenesGRXCR1
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)essv6679918
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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