A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2716728



Internal ID9951016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:6003037..6003169hg38UCSC Ensembl
Outerchr18:6003036..6003168hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6665981, essv6960578, essv6967044, essv6674384, essv6863272
SamplesSSM027, SSM088, SSM031, SSM029, SSM026
Known GenesL3MBTL4
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)esv2716728
Frequency
Sample Size96
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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