A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2721396



Internal ID10305032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:206374381..206375640hg38UCSC Ensembl
Outerchr2:207239105..207240364hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg381260
hg191260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6962280, essv6669705, essv6788266, essv6933779, essv6859731, essv6847736, essv6766855, essv6764465, essv6906580, essv6733784, essv6817122, essv6864517, essv6951008, essv6955519, essv6819920, essv6853921, essv6825474
SamplesSSM027, SSM064, SSM087, SSM009, SSM088, SSM021, SSM026, SSM089, SSM031, SSM014, SSM086, SSM078, SSM080, SSM010, SSM025, SSM049, SSM063
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)esv2721396
Frequency
Sample Size96
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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