A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2748206



Internal ID10329176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:112894648..112895434hg38UCSC Ensembl
Outerchr13:113548962..113549748hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38787
hg19787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6973040, essv6706413, essv6936400, essv6774353, essv6740109, essv6966177, essv6851574, essv6928115, essv6823869, essv6835085, essv6728546, essv6876844, essv6932099, essv6698919, essv6885232, essv6945206, essv6695801, essv6668331, essv6953473, essv6836410, essv6720918, essv6775914, essv6879646, essv6971074, essv6673539, essv6803652
SamplesSSM008, SSM027, SSM046, SSM079, SSM038, SSM073, SSM093, SSM023, SSM028, SSM092, SSM021, SSM019, SSM031, SSM044, SSM086, SSM066, SSM040, SSM082, SSM020, SSM007, SSM037, SSM010, SSM095, SSM025, SSM004, SSM030
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)esv2748206
Frequency
Sample Size96
Observed Gain0
Observed Loss26
Observed Complex0
Frequencyn/a


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