A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2746327



Internal ID10327297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:105496409..105497491hg38UCSC Ensembl
Outerchr12:105890187..105891269hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg381083
hg191083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6827775, essv6823691, essv6876715, essv6940400, essv6945023, essv6783619, essv6709555, essv6732189, essv6716853, essv6977305, essv6970866, essv6772100, essv6779520, essv6691662, essv6842491, essv6959364, essv6702518, essv6787818, essv6894706, essv6845997, essv6936198
SamplesSSM036, SSM079, SSM065, SSM039, SSM041, SSM023, SSM028, SSM092, SSM084, SSM021, SSM047, SSM069, SSM029, SSM026, SSM067, SSM085, SSM068, SSM080, SSM022, SSM043, SSM098
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)esv2746327
Frequency
Sample Size96
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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