A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2720405



Internal ID9954701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:95945275..95951725hg38UCSC Ensembl
Outerchr2:96611023..96617473hg19UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg386451
hg196451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6896091, essv6968333, essv6726190, essv6933676, essv6753770, essv6710924, essv6844175, essv6675542, essv6762045, essv6669524, essv6910412, essv6759315, essv6953017, essv6714590, essv6801879, essv6883504, essv6874977, essv6925991, essv6739116, essv6962094, essv6707570, essv6721399, essv6864381, essv6693162, essv6898878, essv6874978, essv6892637, essv6683122, essv6787453, essv6751664, essv6704161, essv6797825, essv6748044, essv6825353, essv6816979, essv6810581, essv6697233, essv6777279, essv6938037, essv6879787, essv6871983, essv6686440, essv6917788, essv6972972, essv6847567, essv6807635, essv6718496, essv6781248, essv6919740, essv6914272, essv6868983, essv6778598, essv6942200, essv6844176, essv6938036, essv6836525, essv6902851
SamplesSSM100, SSM008, SSM083, SSM027, SSM075, SSM046, SSM038, SSM013, SSM009, SSM073, SSM042, SSM041, SSM023, SSM058, SSM028, SSM092, SSM090, SSM021, SSM061, SSM029, SSM062, SSM089, SSM017, SSM019, SSM035, SSM032, SSM003, SSM031, SSM067, SSM044, SSM001, SSM086, SSM085, SSM068, SSM040, SSM072, SSM007, SSM015, SSM078, SSM016, SSM080, SSM037, SSM076, SSM022, SSM091, SSM095, SSM034, SSM004, SSM099, SSM043, SSM052, SSM098, SSM056, SSM012
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)esv2720405
Frequency
Sample Size96
Observed Gain0
Observed Loss54
Observed Complex0
Frequencyn/a


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