A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2731095



Internal ID9965412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:3060832..3061535hg38UCSC Ensembl
Outerchr10:3103024..3103727hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38704
hg19704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6708843, essv6677461, essv6735587, essv6935726, essv6927616, essv6900359, essv6850600, essv6806105, essv6705884, essv6720339, essv6906041, essv6965179, essv6749402, essv6856622, essv6809101, essv6827332, essv6923940, essv6691293, essv6870462, essv6890952, essv6948690, essv6842093, essv6900358, essv6976452, essv6861928, essv6811947, essv6830967, essv6894342, essv6771716
SamplesSSM100, SSM036, SSM027, SSM024, SSM075, SSM065, SSM087, SSM097, SSM074, SSM088, SSM002, SSM084, SSM090, SSM021, SSM018, SSM029, SSM019, SSM032, SSM044, SSM086, SSM006, SSM081, SSM040, SSM007, SSM080, SSM076, SSM098, SSM056
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)esv2731095
Frequency
Sample Size96
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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