A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2734954



Internal ID5045686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:103463074..103463392hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv6708705, essv6676896, essv6887276, essv6893838, essv6865989, essv6881668, essv6805706, essv6826734, essv6957559, essv6890491, essv6943808, essv6899960, essv6861269, essv6684283, essv6964257, essv6671622, essv6907916, essv6795003, essv6849658, essv6975365, essv6870036, essv6799212, essv6855718, essv6786752, essv6904024, essv6701440, essv6818612, essv6837755, essv6857987
SamplesSSM027, SSM013, SSM086, SSM078, SSM088, SSM089, SSM090, SSM031, SSM072, SSM071, SSM032, SSM039, SSM094, SSM083, SSM097, SSM041, SSM100, SSM011, SSM029, SSM069, SSM034, SSM087, SSM096, SSM023, SSM074, SSM026, SSM014, SSM098, SSM080
Known GenesRELN
Method
Analysis
PlatformIllumina HiSeq2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2734954
Frequency
Sample Size96
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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