A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2734989



Internal ID5045721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:107409817..107411018hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv6762830, essv6751855, essv6865995, essv6690768, essv6705754, essv6734582, essv6798376, essv6935086, essv6975375, essv6841558, essv6873036, essv6818619, essv6763697, essv6765215, essv6712156, essv6975594, essv6731154, essv6805713, essv6760286, essv6828364, essv6911649, essv6771135, essv6743391, essv6931562, essv6746171, essv6890632, essv6754807, essv6957569, essv6740278, essv6748984, essv6778539
SamplesSSM010, SSM065, SSM007, SSM053, SSM006, SSM036, SSM055, SSM091, SSM084, SSM061, SSM042, SSM078, SSM089, SSM057, SSM001, SSM067, SSM062, SSM012, SSM056, SSM009, SSM029, SSM003, SSM021, SSM063, SSM052, SSM074, SSM015, SSM026, SSM049, SSM008, SSM058
Known GenesSLC26A3
Method
Analysis
PlatformIllumina HiSeq2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2734989
Frequency
Sample Size96
Observed Gain0
Observed Loss31
Observed Complex0
Frequencyn/a


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