A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6764632



Internal ID9826228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:2430201..2430463hg38UCSC Ensembl
Outerchr4:2431928..2432190hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2726846, esv2726835
Supporting Variants
SamplesSSM063
Known GenesLOC402160
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)essv6764632
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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