A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2734469



Internal ID9968796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:56694221..56702248hg38UCSC Ensembl
Outerchr7:56761914..56769941hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg388028
hg198028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6884423, essv6857098, essv6786678, essv6740227, essv6805649, essv6948075, essv6814564, essv6671516, essv6915275, essv6774817, essv6737164, essv6698084, essv6802760, essv6751804, essv6890066, essv6830408, essv6890415, essv6849530, essv6767747, essv6939293, essv6762787, essv6778462, essv6727367
SamplesSSM024, SSM046, SSM011, SSM064, SSM038, SSM097, SSM073, SSM050, SSM074, SSM057, SSM069, SSM062, SSM031, SSM067, SSM086, SSM066, SSM081, SSM016, SSM077, SSM022, SSM095, SSM052, 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)esv2734469
Frequency
Sample Size96
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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