A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2734899



Internal ID9969229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:100608933..100609271hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6931429, essv6887270, essv6857932, essv6890482, essv6964245, essv6907910, essv6923379, essv6731043, essv6684279, essv6969734, essv6893829, essv6705327, essv6855707, essv6957547, essv6963929, essv6935077, essv6794994, essv6774863, essv6849646, essv6814617
SamplesSSM071, SSM027, SSM011, SSM087, SSM097, SSM028, SSM021, SSM018, SSM096, SSM026, SSM003, SSM014, SSM086, SSM066, SSM040, SSM007, SSM077, SSM034, SSM004, SSM098
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)esv2734899
Frequency
Sample Size96
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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