A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6899295



Internal ID10292648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:73543202..73543478hg38UCSC Ensembl
Outerchr4:74408919..74409195hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2727826, esv2727828, esv2727831
Supporting Variants
SamplesSSM100
Known Genes
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)essv6899295
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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