A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2732867



Internal ID9967189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:149964506..149965727hg38UCSC Ensembl
Outerchr6:150285642..150286863hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381222
hg191222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6740080, essv6765099, essv6845052, essv6762717, essv6719550, essv6962706, essv6704587, essv6796554, essv6761886, essv6865718, essv6746032, essv6754646, essv6934844, essv6826887, essv6818373, essv6794768, essv6774679, essv6743260, essv6833873, essv6767627, essv6963901, essv6841359, essv6974972
SamplesSSM008, SSM071, SSM027, SSM064, SSM009, SSM058, SSM084, SSM021, SSM029, SSM062, SSM089, SSM044, SSM001, SSM066, SSM006, SSM085, SSM082, SSM078, SSM053, SSM010, SSM055, SSM052, SSM063
Known GenesULBP1
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)esv2732867
Frequency
Sample Size96
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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