A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6883852



Internal ID9932087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:70926143..70934315hg38UCSC Ensembl
Outerchr4:71791860..71800032hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg388173
hg198173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2727796
Supporting Variants
SamplesSSM095
Known GenesMOB1B
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)essv6883852
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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