A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2716692



Internal ID9950980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:3674687..3675088hg38UCSC Ensembl
Outerchr18:3674687..3675088hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6772850, essv6713675, essv6820549, essv6960568, essv6852394, essv6863266, essv6828446, essv6674375, essv6721435, essv6665970, essv6868081, essv6804034, essv6858363, essv6921019, essv6967035
SamplesSSM027, SSM065, SSM087, SSM073, SSM042, SSM088, SSM029, SSM026, SSM089, SSM017, SSM031, SSM044, SSM086, SSM078, SSM080
Known GenesDLGAP1
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)esv2716692
Frequency
Sample Size96
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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