A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2737651



Internal ID10321287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:63664773..63672828hg38UCSC Ensembl
Outerchr10:65424533..65432588hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg388056
hg198056
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6948758, essv6935802, essv6887776, essv6834628, essv6734986, essv6672674, essv6842149, essv6915873, essv6876436, essv6831023, essv6731812, essv6736065, essv6681307, essv6702376, essv6906562, essv6775434
SamplesSSM024, SSM002, SSM092, SSM084, SSM021, SSM047, SSM096, SSM031, SSM001, SSM033, SSM066, SSM081, SSM082, SSM007, SSM016, SSM049
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)esv2737651
Frequency
Sample Size96
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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